Canonical Allele Identifier: CA2326525575

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18786132T= , CM000681.2:g.18786132T=	GRCh38
NC_000019.9:g.18896942T= , CM000681.1:g.18896942T=	GRCh37
NC_000019.8:g.18757942T=	NCBI36
NG_007070.1:g.10173A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000222271.7:c.1322A= MANE Select	ENSP00000222271.2:p.His441=
ENST00000222271.6:c.1322A=	ENSP00000222271.2:p.His441=
ENST00000425807.1:c.1163A=	ENSP00000403792.1:p.His388=
ENST00000542601.6:c.1223A=	ENSP00000439156.2:p.His408=
ENST00000612179.1:n.572A=
NM_000095.2:c.1322A=	NP_000086.2:p.His441=
NM_000095.3:c.1322A= MANE Select	NP_000086.2:p.His441=