Canonical Allele Identifier: CA2326524946

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18785077T= , CM000681.2:g.18785077T=	GRCh38
NC_000019.9:g.18895887T= , CM000681.1:g.18895887T=	GRCh37
NC_000019.8:g.18756887T=	NCBI36
NG_007070.1:g.11228A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1733A= MANE Select	ENSP00000222271.2:p.Asn578=
ENST00000222271.6:c.1733A=	ENSP00000222271.2:p.Asn578=
ENST00000425807.1:c.1574A=	ENSP00000403792.1:p.Asn525=
ENST00000542601.6:c.1634A=	ENSP00000439156.2:p.Asn545=
NM_000095.2:c.1733A=	NP_000086.2:p.Asn578=
NM_000095.3:c.1733A= MANE Select	NP_000086.2:p.Asn578=