Canonical Allele Identifier: CA2326525569

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18786120C= , CM000681.2:g.18786120C=	GRCh38
NC_000019.9:g.18896930C= , CM000681.1:g.18896930C=	GRCh37
NC_000019.8:g.18757930C=	NCBI36
NG_007070.1:g.10185G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000222271.7:c.1334G= MANE Select	ENSP00000222271.2:p.Arg445=
ENST00000222271.6:c.1334G=	ENSP00000222271.2:p.Arg445=
ENST00000425807.1:c.1175G=	ENSP00000403792.1:p.Arg392=
ENST00000542601.6:c.1235G=	ENSP00000439156.2:p.Arg412=
ENST00000612179.1:n.584G=
NM_000095.2:c.1334G=	NP_000086.2:p.Arg445=
NM_000095.3:c.1334G= MANE Select	NP_000086.2:p.Arg445=