Canonical Allele Identifier: CA2326526223

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18787281C= , CM000681.2:g.18787281C=	GRCh38
NC_000019.9:g.18898090C= , CM000681.1:g.18898090C=	GRCh37
NC_000019.8:g.18759090C=	NCBI36
NG_007070.1:g.9025G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1135+210G= MANE Select	ENSP00000222271.2:n.1135+210G=
ENST00000222271.6:c.1135+210G=	ENSP00000222271.2:n.1135+210G=
ENST00000425807.1:c.976+210G=	ENSP00000403792.1:n.976+210G=
ENST00000542601.6:c.1036+210G=	ENSP00000439156.2:n.1036+210G=
NM_000095.2:c.1135+210G=	NP_000086.2:n.1135+210G=
NM_000095.3:c.1135+210G= MANE Select	NP_000086.2:n.1135+210G=