Canonical Allele Identifier: CA2326524924

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18785030C= , CM000681.2:g.18785030C=	GRCh38
NC_000019.9:g.18895840C= , CM000681.1:g.18895840C=	GRCh37
NC_000019.8:g.18756840C=	NCBI36
NG_007070.1:g.11275G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1780G= MANE Select	ENSP00000222271.2:p.Asp594=
ENST00000222271.6:c.1780G=	ENSP00000222271.2:p.Asp594=
ENST00000425807.1:c.1621G=	ENSP00000403792.1:p.Asp541=
ENST00000542601.6:c.1681G=	ENSP00000439156.2:p.Asp561=
NM_000095.2:c.1780G=	NP_000086.2:p.Asp594=
NM_000095.3:c.1780G= MANE Select	NP_000086.2:p.Asp594=