Canonical Allele Identifier: CA2326525548

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18786055C= , CM000681.2:g.18786055C=	GRCh38
NC_000019.9:g.18896865C= , CM000681.1:g.18896865C=	GRCh37
NC_000019.8:g.18757865C=	NCBI36
NG_007070.1:g.10250G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1399G= MANE Select	ENSP00000222271.2:p.Ala467=
ENST00000222271.6:c.1399G=	ENSP00000222271.2:p.Ala467=
ENST00000425807.1:c.1240G=	ENSP00000403792.1:p.Ala414=
ENST00000542601.6:c.1300G=	ENSP00000439156.2:p.Ala434=
NM_000095.2:c.1399G=	NP_000086.2:p.Ala467=
NM_000095.3:c.1399G= MANE Select	NP_000086.2:p.Ala467=