Canonical Allele Identifier: CA2326527271

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18789260A= , CM000681.2:g.18789260A=	GRCh38
NC_000019.9:g.18900069A= , CM000681.1:g.18900069A=	GRCh37
NC_000019.8:g.18761069A=	NCBI36
NG_007070.1:g.7046T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.428T= MANE Select	ENSP00000222271.2:p.Ile143=
ENST00000222271.6:c.428T=	ENSP00000222271.2:p.Ile143=
ENST00000425807.1:c.391-368T=	ENSP00000403792.1:n.391-368T=
ENST00000542601.6:c.329T=	ENSP00000439156.2:p.Ile110=
NM_000095.2:c.428T=	NP_000086.2:p.Ile143=
NM_000095.3:c.428T= MANE Select	NP_000086.2:p.Ile143=