Canonical Allele Identifier: CA2326525577

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18786136C= , CM000681.2:g.18786136C=	GRCh38
NC_000019.9:g.18896946C= , CM000681.1:g.18896946C=	GRCh37
NC_000019.8:g.18757946C=	NCBI36
NG_007070.1:g.10169G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1318G= MANE Select	ENSP00000222271.2:p.Gly440=
ENST00000222271.6:c.1318G=	ENSP00000222271.2:p.Gly440=
ENST00000425807.1:c.1159G=	ENSP00000403792.1:p.Gly387=
ENST00000542601.6:c.1219G=	ENSP00000439156.2:p.Gly407=
ENST00000612179.1:n.568G=
NM_000095.2:c.1318G=	NP_000086.2:p.Gly440=
NM_000095.3:c.1318G= MANE Select	NP_000086.2:p.Gly440=