Canonical Allele Identifier: CA1396604262

Gene: CD80

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119542097A= , CM000665.2:g.119542097A=	GRCh38
NC_000003.11:g.119260944A= , CM000665.1:g.119260944A=	GRCh37
NC_000003.10:g.120743634A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264246.8:c.418+2453T= MANE Select	ENSP00000264246.3:n.418+2453T=
ENST00000264246.7:c.418+2453T=	ENSP00000264246.3:n.418+2453T=
ENST00000383669.3:c.418+2453T=	ENSP00000373165.3:n.418+2453T=
ENST00000478182.5:c.418+2453T=	ENSP00000418364.1:n.418+2453T=
NM_005191.3:c.418+2453T=	NP_005182.1:n.418+2453T=
XM_011513325.1:c.418+2453T=	XP_011511627.1:n.418+2453T=
XM_011513326.1:c.418+2453T=	XP_011511628.1:n.418+2453T=
XM_011513327.1:c.205+2453T=	XP_011511629.1:n.205+2453T=
XM_011513327.2:c.205+2453T=	XP_011511629.1:n.205+2453T=
XM_017007520.2:c.418+2453T=	XP_016863009.1:n.418+2453T=
NM_005191.4:c.418+2453T= MANE Select	NP_005182.1:n.418+2453T=