Canonical Allele Identifier: CA2326525580

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18786141C= , CM000681.2:g.18786141C=	GRCh38
NC_000019.9:g.18896951C= , CM000681.1:g.18896951C=	GRCh37
NC_000019.8:g.18757951C=	NCBI36
NG_007070.1:g.10164G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000222271.7:c.1313G= MANE Select	ENSP00000222271.2:p.Gly438=
ENST00000222271.6:c.1313G=	ENSP00000222271.2:p.Gly438=
ENST00000425807.1:c.1154G=	ENSP00000403792.1:p.Gly385=
ENST00000542601.6:c.1214G=	ENSP00000439156.2:p.Gly405=
ENST00000612179.1:n.563G=
NM_000095.2:c.1313G=	NP_000086.2:p.Gly438=
NM_000095.3:c.1313G= MANE Select	NP_000086.2:p.Gly438=