Canonical Allele Identifier: CA2326525660

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18786269A= , CM000681.2:g.18786269A=	GRCh38
NC_000019.9:g.18897079A= , CM000681.1:g.18897079A=	GRCh37
NC_000019.8:g.18758079A=	NCBI36
NG_007070.1:g.10036T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1277T= MANE Select	ENSP00000222271.2:p.Val426=
ENST00000222271.6:c.1277T=	ENSP00000222271.2:p.Val426=
ENST00000425807.1:c.1118T=	ENSP00000403792.1:p.Val373=
ENST00000542601.6:c.1178T=	ENSP00000439156.2:p.Val393=
ENST00000612179.1:n.527T=
NM_000095.2:c.1277T=	NP_000086.2:p.Val426=
NM_000095.3:c.1277T= MANE Select	NP_000086.2:p.Val426=