Canonical Allele Identifier: CA2326525573

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18786129T= , CM000681.2:g.18786129T=	GRCh38
NC_000019.9:g.18896939T= , CM000681.1:g.18896939T=	GRCh37
NC_000019.8:g.18757939T=	NCBI36
NG_007070.1:g.10176A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000222271.7:c.1325A= MANE Select	ENSP00000222271.2:p.Gln442=
ENST00000222271.6:c.1325A=	ENSP00000222271.2:p.Gln442=
ENST00000425807.1:c.1166A=	ENSP00000403792.1:p.Gln389=
ENST00000542601.6:c.1226A=	ENSP00000439156.2:p.Gln409=
ENST00000612179.1:n.575A=
NM_000095.2:c.1325A=	NP_000086.2:p.Gln442=
NM_000095.3:c.1325A= MANE Select	NP_000086.2:p.Gln442=