Canonical Allele Identifier: CA404887780
Gene: COMP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787507G>T , CM000681.2:g.18787507G>T GRCh38
NC_000019.9:g.18898316G>T , CM000681.1:g.18898316G>T GRCh37
NC_000019.8:g.18759316G>T NCBI36
NG_007070.1:g.8799C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000222271.7:c.1119C>A MANE Select ENSP00000222271.2:p.Asp373Glu
ENST00000222271.6:c.1119C>A ENSP00000222271.2:p.Asp373Glu
ENST00000425807.1:c.960C>A ENSP00000403792.1:p.Asp320Glu
ENST00000542601.6:c.1020C>A ENSP00000439156.2:p.Asp340Glu
NM_000095.2:c.1119C>A NP_000086.2:p.Asp373Glu
NM_000095.3:c.1119C>A MANE Select NP_000086.2:p.Asp373Glu