Canonical Allele Identifier: CA2326524919

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18785019C= , CM000681.2:g.18785019C=	GRCh38
NC_000019.9:g.18895829C= , CM000681.1:g.18895829C=	GRCh37
NC_000019.8:g.18756829C=	NCBI36
NG_007070.1:g.11286G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1791G= MANE Select	ENSP00000222271.2:p.Ala597=
ENST00000222271.6:c.1791G=	ENSP00000222271.2:p.Ala597=
ENST00000425807.1:c.1632G=	ENSP00000403792.1:p.Ala544=
ENST00000542601.6:c.1692G=	ENSP00000439156.2:p.Ala564=
NM_000095.2:c.1791G=	NP_000086.2:p.Ala597=
NM_000095.3:c.1791G= MANE Select	NP_000086.2:p.Ala597=