Canonical Allele Identifier: CA2326525510

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18785985G= , CM000681.2:g.18785985G=	GRCh38
NC_000019.9:g.18896795G= , CM000681.1:g.18896795G=	GRCh37
NC_000019.8:g.18757795G=	NCBI36
NG_007070.1:g.10320C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1469C= MANE Select	ENSP00000222271.2:p.Pro490=
ENST00000222271.6:c.1469C=	ENSP00000222271.2:p.Pro490=
ENST00000425807.1:c.1310C=	ENSP00000403792.1:p.Pro437=
ENST00000542601.6:c.1370C=	ENSP00000439156.2:p.Pro457=
NM_000095.2:c.1469C=	NP_000086.2:p.Pro490=
NM_000095.3:c.1469C= MANE Select	NP_000086.2:p.Pro490=