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Genome Displays Related Resources Gene HomoloGene MANE RefSeq
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Report for CCDS35297.1 (current version)
CCDS |
Status |
Species |
Chrom. |
Gene |
CCDS Release |
NCBI Annotation Release |
Ensembl Annotation Release |
Links |
35297.1 |
Public |
Homo sapiens |
X |
FAM156A |
24 |
110 |
108 |
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Public since: CCDS release 3, NCBI annotation release 36.2, Ensembl annotation release 41
Review status: Reviewed (by RefSeq and Havana) Sequence IDs included in CCDS 35297.1
Original |
Current |
Source |
Nucleotide ID |
Protein ID |
MANE |
Status in CCDS |
Seq. Status |
Links |
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|
EBI |
ENST00000596733.7 |
ENSP00000471676.1 |
|
Accepted |
alive |
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EBI |
ENST00000622323.5 |
ENSP00000477905.2 |
|
Accepted |
alive |
|
|
|
EBI |
ENST00000615092.4 |
ENSP00000479184.1 |
|
Accepted |
alive |
|
|
|
EBI |
ENST00000622732.5 |
ENSP00000479338.2 |
|
Accepted |
alive |
|
|
|
EBI |
ENST00000612846.5 |
ENSP00000479348.2 |
|
Accepted |
alive |
|
|
|
EBI |
ENST00000619586.5 |
ENSP00000479822.2 |
|
Accepted |
alive |
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EBI |
ENST00000613284.1 |
ENSP00000480373.1 |
|
Accepted |
alive |
|
|
|
EBI |
ENST00000611661.4 |
ENSP00000480518.1 |
|
Accepted |
alive |
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|
EBI |
ENST00000617970.4 |
ENSP00000481435.1 |
|
Accepted |
alive |
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EBI |
ENST00000622197.5 |
ENSP00000481568.2 |
|
Accepted |
alive |
|
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|
EBI |
ENST00000622447.5 |
ENSP00000482142.1 |
MANE Select |
Accepted |
alive |
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|
EBI |
ENST00000619518.5 |
ENSP00000482562.2 |
|
Accepted |
alive |
|
|
|
EBI |
ENST00000618601.5 |
ENSP00000482980.2 |
|
Accepted |
alive |
|
|
|
EBI |
ENST00000612915.4 |
ENSP00000484167.1 |
|
Accepted |
alive |
|
|
|
EBI |
ENST00000610625.5 |
ENSP00000484486.2 |
|
Accepted |
alive |
|
|
|
EBI |
ENST00000619373.5 |
ENSP00000484757.2 |
|
Accepted |
alive |
|
|
|
EBI |
ENST00000612083.5 |
ENSP00000484967.2 |
|
Accepted |
alive |
|
|
|
EBI |
ENST00000623782.3 |
ENSP00000485247.1 |
|
Accepted |
alive |
|
|
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NCBI |
NM_001242489.2 |
NP_001229418.1 |
|
Accepted |
alive |
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|
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NCBI |
NM_001242490.2 |
NP_001229419.1 |
|
Accepted |
alive |
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NCBI |
NM_001242491.1 |
NP_001229420.1 |
|
Accepted |
alive |
|
|
|
NCBI |
NM_001242492.2 |
NP_001229421.1 |
|
Accepted |
alive |
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|
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NCBI |
NM_001242493.2 |
NP_001229422.1 |
|
Accepted |
alive |
|
|
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NCBI |
NM_001242494.2 |
NP_001229423.1 |
|
Accepted |
alive |
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|
NCBI |
NM_001242495.2 |
NP_001229424.1 |
|
Accepted |
alive |
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|
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NCBI |
NM_001242496.2 |
NP_001229425.1 |
|
Accepted |
alive |
|
|
|
NCBI |
NM_001242497.2 |
NP_001229426.1 |
|
Accepted |
alive |
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|
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NCBI |
NM_001377060.1 |
NP_001363989.1 |
|
Accepted |
alive |
|
|
|
NCBI |
NM_001377061.1 |
NP_001363990.1 |
|
Accepted |
alive |
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NCBI |
NM_001377062.1 |
NP_001363991.1 |
|
Accepted |
alive |
|
|
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NCBI |
NM_001377063.1 |
NP_001363992.1 |
|
Accepted |
alive |
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NCBI |
NM_001387706.1 |
NP_001374635.1 |
MANE Select |
Accepted |
alive |
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NCBI |
NM_014138.5 |
NP_054857.2 |
|
Accepted |
alive |
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Chromosomal Locations for CCDS 35297.1
Assembly GRCh38.p14 (GCF_000001405.40)
CCDS Sequence Data |
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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 (642 nt): ATGGATCCACTCCAGAAACGGAATCCAGCATCGCCTTCCAAATCTTCCCCGATGACAGCTGCAGAGACTT CCCAGGAAGGTCCAGCGCCCTCTCAGCCTTCGTACTCAGAACAGCCGATGATGGGCCTCAGTAACCTGAG CCCCGGTCCTGGCCCCAGCCAGGCCGTGCCTCTCCCAGAGGGGCTGCTCCGCCAGCGGTACAGAGAGGAG AAGACCCTGGAAGAGCGGCGGTGGGAGAGGCTGGAGTTCCTTCAGAGGAAGAAAGCATTCCTGCGGCATG TGAGGAGGAGACACCGCGATCACATGGCCCCCTATGCTGTTGGGAGGGAAGCCAGAATCTCCCCATTAGG TGACAGAAGTCAGAATCGATTCCGATGTGAATGTCGATACTGCCAGAGCCACAGGCCGAATCTTTCTGGG ATCCCTGGGGAGAGTAACAGGGCCCCACATCCCTCCTCCTGGGAGACGCTGGTGCAGGGCCTCAGTGGCT TGACTCTCAGCCTAGGCACCAACCAGCCCGGGCCTCTGCCTGAAGCGGCACTCCAGCCACAGGAGACAGA GGAGAAGCGCCAGCGAGAGAGGCAGCAGGAGAGCAAAATAATGTTTCAGAGGCTGCTCAAGCAGTGGTTA GAGGAAAACTGA
Translation (213 aa): MDPLQKRNPASPSKSSPMTAAETSQEGPAPSQPSYSEQPMMGLSNLSPGPGPSQAVPLPEGLLRQRYREE KTLEERRWERLEFLQRKKAFLRHVRRRHRDHMAPYAVGREARISPLGDRSQNRFRCECRYCQSHRPNLSG IPGESNRAPHPSSWETLVQGLSGLTLSLGTNQPGPLPEAALQPQETEEKRQRERQQESKIMFQRLLKQWL EEN
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