Canonical Allele Identifier: CA2326524018

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18783139G= , CM000681.2:g.18783139G=	GRCh38
NC_000019.9:g.18893949G= , CM000681.1:g.18893949G=	GRCh37
NC_000019.8:g.18754949G=	NCBI36
NG_007070.1:g.13166C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.2142C= MANE Select	ENSP00000222271.2:p.Asp714=
ENST00000222271.6:c.2142C=	ENSP00000222271.2:p.Asp714=
ENST00000425807.1:c.1983C=	ENSP00000403792.1:p.Asp661=
ENST00000542601.6:c.2043C=	ENSP00000439156.2:p.Asp681=
NM_000095.2:c.2142C=	NP_000086.2:p.Asp714=
NM_000095.3:c.2142C= MANE Select	NP_000086.2:p.Asp714=