Canonical Allele Identifier: CA404884296
Gene: COMP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18786003C>T , CM000681.2:g.18786003C>T GRCh38
NC_000019.9:g.18896813C>T , CM000681.1:g.18896813C>T GRCh37
NC_000019.8:g.18757813C>T NCBI36
NG_007070.1:g.10302G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000222271.7:c.1451G>A MANE Select ENSP00000222271.2:p.Cys484Tyr
ENST00000222271.6:c.1451G>A ENSP00000222271.2:p.Cys484Tyr
ENST00000425807.1:c.1292G>A ENSP00000403792.1:p.Cys431Tyr
ENST00000542601.6:c.1352G>A ENSP00000439156.2:p.Cys451Tyr
NM_000095.2:c.1451G>A NP_000086.2:p.Cys484Tyr
NM_000095.3:c.1451G>A MANE Select NP_000086.2:p.Cys484Tyr