Canonical Allele Identifier: CA404885020
Gene: COMP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18786102A>T , CM000681.2:g.18786102A>T GRCh38
NC_000019.9:g.18896912A>T , CM000681.1:g.18896912A>T GRCh37
NC_000019.8:g.18757912A>T NCBI36
NG_007070.1:g.10203T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000222271.7:c.1352T>A MANE Select ENSP00000222271.2:p.Val451Glu
ENST00000222271.6:c.1352T>A ENSP00000222271.2:p.Val451Glu
ENST00000425807.1:c.1193T>A ENSP00000403792.1:p.Val398Glu
ENST00000542601.6:c.1253T>A ENSP00000439156.2:p.Val418Glu
NM_000095.2:c.1352T>A NP_000086.2:p.Val451Glu
NM_000095.3:c.1352T>A MANE Select NP_000086.2:p.Val451Glu