Canonical Allele Identifier: CA2326524943

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18785073G= , CM000681.2:g.18785073G=	GRCh38
NC_000019.9:g.18895883G= , CM000681.1:g.18895883G=	GRCh37
NC_000019.8:g.18756883G=	NCBI36
NG_007070.1:g.11232C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1737C= MANE Select	ENSP00000222271.2:p.Gly579=
ENST00000222271.6:c.1737C=	ENSP00000222271.2:p.Gly579=
ENST00000425807.1:c.1578C=	ENSP00000403792.1:p.Gly526=
ENST00000542601.6:c.1638C=	ENSP00000439156.2:p.Gly546=
NM_000095.2:c.1737C=	NP_000086.2:p.Gly579=
NM_000095.3:c.1737C= MANE Select	NP_000086.2:p.Gly579=