Canonical Allele Identifier: CA2326527258

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18789231C= , CM000681.2:g.18789231C=	GRCh38
NC_000019.9:g.18900040C= , CM000681.1:g.18900040C=	GRCh37
NC_000019.8:g.18761040C=	NCBI36
NG_007070.1:g.7075G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.457G= MANE Select	ENSP00000222271.2:p.Ala153=
ENST00000222271.6:c.457G=	ENSP00000222271.2:p.Ala153=
ENST00000425807.1:c.391-339G=	ENSP00000403792.1:n.391-339G=
ENST00000542601.6:c.358G=	ENSP00000439156.2:p.Ala120=
NM_000095.2:c.457G=	NP_000086.2:p.Ala153=
NM_000095.3:c.457G= MANE Select	NP_000086.2:p.Ala153=