Canonical Allele Identifier: CA2326525339

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18785716T= , CM000681.2:g.18785716T=	GRCh38
NC_000019.9:g.18896526T= , CM000681.1:g.18896526T=	GRCh37
NC_000019.8:g.18757526T=	NCBI36
NG_007070.1:g.10589A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000222271.7:c.1625A= MANE Select	ENSP00000222271.2:p.Glu542=
ENST00000222271.6:c.1625A=	ENSP00000222271.2:p.Glu542=
ENST00000425807.1:c.1466A=	ENSP00000403792.1:p.Glu489=
ENST00000542601.6:c.1526A=	ENSP00000439156.2:p.Glu509=
NM_000095.2:c.1625A=	NP_000086.2:p.Glu542=
NM_000095.3:c.1625A= MANE Select	NP_000086.2:p.Glu542=