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Report for CCDS6794.2 (current version)

CCDS Status Species Chrom. Gene CCDS Release NCBI Annotation Release Ensembl Annotation Release Links
6794.2 Public Homo sapiens 9 ALAD 24 110 108 CCDS HistoryNCBI Gene:210Re-query CCDS DB by CCDS ID:6794.2See the combined annotation on chromosome 9 in Sequence Viewer

Public Note for CCDS 6794.1
The coding region has been updated to start at an alternate in-frame start codon that is supported by conservation data or a publication. PMID:3463993 suggests that the downstream AUG codon is the translation start site from evidence provided by N-terminal sequencing of the human protein. Although this may be the dominant translation start site, it is possible that some translation also occurs from the upstream AUG which is 27 nt upstream of the annotated start for this CCDS. The upstream AUG is in a weak Kozak context so a possible mechanism is that leaky scanning by ribosomes occurs so that, in most cases, ribosomes continue scanning and use the downstream AUG as the translation initiation site.

Public since: CCDS release 1, NCBI annotation release 35.1, Ensembl annotation release 23

Review status: Reviewed (by RefSeq, Havana and CCDS collaboration)


Attributes
CDS uses downstream AUG

Sequence IDs included in CCDS 6794.2

Original Current Source Nucleotide ID Protein ID MANE Status in CCDS Seq. Status Links
Original member Current member EBI ENST00000409155.8 ENSP00000386284.3 MANE Select Accepted alive Link to Ensembl Transcript Viewer:ENST00000409155.8Link to Ensembl Protein Viewer:ENSP00000386284.3Re-query CCDS DB by Nucleotide ID:ENST00000409155Re-query CCDS DB by Protein ID:ENSP00000386284
Original member Current member NCBI NM_000031.6 NP_000022.3 MANE Select Accepted alive Link to Nucleotide Sequence:NM_000031.6Link to Protein Sequence:NP_000022.3Re-query CCDS DB by Nucleotide ID:NM_000031Re-query CCDS DB by Protein ID:NP_000022Link to BLAST:NP_000022.3

RefSeq Length Related UniProtKB/SwissProt Length Identity Gaps Mismatches
NP_000022.3 330 P13716-1 330 100% 0 0

Chromosomal Locations for CCDS 6794.2

Assembly GRCh38.p14 (GCF_000001405.40)

On '-' strand of Chromosome 9 (NC_000009.12)
Genome Browser links: Link to NCBI NucleotideLink to UCSC Genome Browser on chromosome 9Link to Ensembl Genome Browser on chromosome 9See the combined annotation on chromosome 9 in Sequence Viewer

Chromosome Start Stop Links
9 113388300 113388361 Link to NCBI NucleotideLink to UCSC Genome Browser on chromosome 9Link to Ensembl Genome Browser on chromosome 9
9 113388977 113389106 Link to NCBI NucleotideLink to UCSC Genome Browser on chromosome 9Link to Ensembl Genome Browser on chromosome 9
9 113389438 113389524 Link to NCBI NucleotideLink to UCSC Genome Browser on chromosome 9Link to Ensembl Genome Browser on chromosome 9
9 113389599 113389686 Link to NCBI NucleotideLink to UCSC Genome Browser on chromosome 9Link to Ensembl Genome Browser on chromosome 9
9 113389773 113389828 Link to NCBI NucleotideLink to UCSC Genome Browser on chromosome 9Link to Ensembl Genome Browser on chromosome 9
9 113390405 113390493 Link to NCBI NucleotideLink to UCSC Genome Browser on chromosome 9Link to Ensembl Genome Browser on chromosome 9
9 113390593 113390676 Link to NCBI NucleotideLink to UCSC Genome Browser on chromosome 9Link to Ensembl Genome Browser on chromosome 9
9 113390798 113390933 Link to NCBI NucleotideLink to UCSC Genome Browser on chromosome 9Link to Ensembl Genome Browser on chromosome 9
9 113391527 113391623 Link to NCBI NucleotideLink to UCSC Genome Browser on chromosome 9Link to Ensembl Genome Browser on chromosome 9
9 113392119 113392169 Link to NCBI NucleotideLink to UCSC Genome Browser on chromosome 9Link to Ensembl Genome Browser on chromosome 9
9 113393447 113393559 Link to NCBI NucleotideLink to UCSC Genome Browser on chromosome 9Link to Ensembl Genome Browser on chromosome 9

CCDS Sequence Data
Blue highlighting indicates alternating exons.
Red highlighting indicates amino acids encoded across a splice junction.
 
Mouse over the nucleotide or protein sequence below and click on the highlighted codon or residue to select the pair.

Nucleotide Sequence (993 nt):
ATGCAGCCCCAGTCCGTTCTGCACAGCGGCTACTTCCACCCACTACTTCGGGCCTGGCAGACAGCCACCA
CC
ACCCTCAATGCCTCCAACCTCATCTACCCCATCTTTGTCACGGATGTTCCTGATGACATACAGCCTAT
C
ACCAGCCTCCCAGGAGTGGCCAGGTATGGTGTGAAGCGGCTGGAAGAGATGCTGAGGCCCTTGGTGGAA
GAG
GGCCTACGCTGTGTCTTGATCTTTGGCGTCCCCAGCAGAGTTCCCAAGGACGAGCGGGGTTCCGCAG
CT
GACTCCGAGGAGTCCCCAGCTATTGAGGCAATCCATCTGTTGAGGAAGACCTTCCCCAACCTCCTGGT
G
GCCTGTGATGTCTGCCTGTGTCCCTACACCTCCCATGGTCACTGCGGGCTCCTGAGTGAAAACGGAGCA
TTC
CGGGCTGAGGAGAGCCGCCAGCGGCTGGCTGAGGTGGCATTGGCGTATGCCAAGGCAGGATGTCAGG
TG
GTAGCCCCGTCGGACATGATGGATGGACGCGTGGAAGCCATCAAAGAGGCCCTGATGGCACATGGACT
T
GGCAACAGGGTATCGGTGATGAGCTACAGTGCCAAATTTGCTTCCTGTTTCTATGGCCCTTTCCGGGAT
GCA
GCTAAGTCAAGCCCAGCTTTTGGGGACCGCCGCTGCTACCAGCTGCCCCCTGGAGCACGAGGCCTGG
CT
CTCCGAGCTGTGGACCGGGATGTACGGGAAGGAGCTGACATGCTCATGGTGAAGCCGGGAATGCCCTA
C
CTGGACATCGTGCGGGAGGTAAAGGACAAGCACCCTGACCTCCCTCTCGCCGTGTACCACGTCTCTGGA
GAG
TTTGCCATGCTGTGGCATGGAGCCCAGGCCGGGGCATTTGATCTCAAGGCTGCCGTACTGGAGGCCA
TG
ACTGCCTTCCGCAGAGCAGGTGCTGACATCATCATCACCTACTACACACCGCAGCTGCTGCAGTGGCT
G
AAGGAGGAATGA


Translation (330 aa):
MQPQSVLHSGYFHPLLRAWQTATTTLNASNLIYPIFVTDVPDDIQPITSLPGVARYGVKRLEEMLRPLVE
E
GLRCVLIFGVPSRVPK
DERGSAADSEESPAIEAIHLLRKTFPNLLVACDVCLCPYTSHGHCGLLSENGA
F
RAEESRQRLAEVALAYAKA
GCQVVAPSDMMDGRVEAIKEALMAHGLGNRVSVMSYSAKFASCFYGPFRD
A
AKSSPAFGDRRCYQLPPGARGLALRAV
DRDVREGADMLMVKPGMPYLDIVREVKDKHPDLPLAVYHVSG
E
FAMLWHGAQAGAFDLKAAVLEAMTAFRRA
GADIIITYYTPQLLQWLKEE



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