Canonical Allele Identifier: CA2326525552

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18786072T= , CM000681.2:g.18786072T=	GRCh38
NC_000019.9:g.18896882T= , CM000681.1:g.18896882T=	GRCh37
NC_000019.8:g.18757882T=	NCBI36
NG_007070.1:g.10233A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1382A= MANE Select	ENSP00000222271.2:p.His461=
ENST00000222271.6:c.1382A=	ENSP00000222271.2:p.His461=
ENST00000425807.1:c.1223A=	ENSP00000403792.1:p.His408=
ENST00000542601.6:c.1283A=	ENSP00000439156.2:p.His428=
NM_000095.2:c.1382A=	NP_000086.2:p.His461=
NM_000095.3:c.1382A= MANE Select	NP_000086.2:p.His461=