Canonical Allele Identifier: CA2326525319

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18785672C= , CM000681.2:g.18785672C=	GRCh38
NC_000019.9:g.18896482C= , CM000681.1:g.18896482C=	GRCh37
NC_000019.8:g.18757482C=	NCBI36
NG_007070.1:g.10633G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1668+1G= MANE Select	ENSP00000222271.2:n.1668+1G=
ENST00000222271.6:c.1668+1G=	ENSP00000222271.2:n.1668+1G=
ENST00000425807.1:c.1509+1G=	ENSP00000403792.1:n.1509+1G=
ENST00000542601.6:c.1569+1G=	ENSP00000439156.2:n.1569+1G=
NM_000095.2:c.1668+1G=	NP_000086.2:n.1668+1G=
NM_000095.3:c.1668+1G= MANE Select	NP_000086.2:n.1668+1G=