Canonical Allele Identifier: CA2326527276

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18789277G= , CM000681.2:g.18789277G=	GRCh38
NC_000019.9:g.18900086G= , CM000681.1:g.18900086G=	GRCh37
NC_000019.8:g.18761086G=	NCBI36
NG_007070.1:g.7029C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.411C= MANE Select	ENSP00000222271.2:p.Phe137=
ENST00000222271.6:c.411C=	ENSP00000222271.2:p.Phe137=
ENST00000425807.1:c.391-385C=	ENSP00000403792.1:n.391-385C=
ENST00000542601.6:c.312C=	ENSP00000439156.2:p.Phe104=
NM_000095.2:c.411C=	NP_000086.2:p.Phe137=
NM_000095.3:c.411C= MANE Select	NP_000086.2:p.Phe137=