Canonical Allele Identifier: CA2326526631

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18787996C= , CM000681.2:g.18787996C=	GRCh38
NC_000019.9:g.18898805C= , CM000681.1:g.18898805C=	GRCh37
NC_000019.8:g.18759805C=	NCBI36
NG_007070.1:g.8310G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.975+216G= MANE Select	ENSP00000222271.2:n.975+216G=
ENST00000222271.6:c.975+216G=	ENSP00000222271.2:n.975+216G=
ENST00000425807.1:c.816+216G=	ENSP00000403792.1:n.816+216G=
ENST00000542601.6:c.876+216G=	ENSP00000439156.2:n.876+216G=
NM_000095.2:c.975+216G=	NP_000086.2:n.975+216G=
NM_000095.3:c.975+216G= MANE Select	NP_000086.2:n.975+216G=