Canonical Allele Identifier: CA404887883
Gene: COMP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787519A>T , CM000681.2:g.18787519A>T GRCh38
NC_000019.9:g.18898328A>T , CM000681.1:g.18898328A>T GRCh37
NC_000019.8:g.18759328A>T NCBI36
NG_007070.1:g.8787T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1107T>A MANE Select ENSP00000222271.2:p.Asp369Glu
ENST00000222271.6:c.1107T>A ENSP00000222271.2:p.Asp369Glu
ENST00000425807.1:c.948T>A ENSP00000403792.1:p.Asp316Glu
ENST00000542601.6:c.1008T>A ENSP00000439156.2:p.Asp336Glu
NM_000095.2:c.1107T>A NP_000086.2:p.Asp369Glu
NM_000095.3:c.1107T>A MANE Select NP_000086.2:p.Asp369Glu