Canonical Allele Identifier: CA2326525383

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18785806T= , CM000681.2:g.18785806T=	GRCh38
NC_000019.9:g.18896616T= , CM000681.1:g.18896616T=	GRCh37
NC_000019.8:g.18757616T=	NCBI36
NG_007070.1:g.10499A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1535A= MANE Select	ENSP00000222271.2:p.Lys512=
ENST00000222271.6:c.1535A=	ENSP00000222271.2:p.Lys512=
ENST00000425807.1:c.1376A=	ENSP00000403792.1:p.Lys459=
ENST00000542601.6:c.1436A=	ENSP00000439156.2:p.Lys479=
NM_000095.2:c.1535A=	NP_000086.2:p.Lys512=
NM_000095.3:c.1535A= MANE Select	NP_000086.2:p.Lys512=