Canonical Allele Identifier: CA2326527260

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18789233T= , CM000681.2:g.18789233T=	GRCh38
NC_000019.9:g.18900042T= , CM000681.1:g.18900042T=	GRCh37
NC_000019.8:g.18761042T=	NCBI36
NG_007070.1:g.7073A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.455A= MANE Select	ENSP00000222271.2:p.Glu152=
ENST00000222271.6:c.455A=	ENSP00000222271.2:p.Glu152=
ENST00000425807.1:c.391-341A=	ENSP00000403792.1:n.391-341A=
ENST00000542601.6:c.356A=	ENSP00000439156.2:p.Glu119=
NM_000095.2:c.455A=	NP_000086.2:p.Glu152=
NM_000095.3:c.455A= MANE Select	NP_000086.2:p.Glu152=