Canonical Allele Identifier: CA1397810699

Gene: CD86

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122119486T= , CM000665.2:g.122119486T=	GRCh38
NC_000003.11:g.121838333T= , CM000665.1:g.121838333T=	GRCh37
NC_000003.10:g.123321023T=	NCBI36
NG_029928.1:g.69125T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330540.7:c.942T= MANE Select	ENSP00000332049.2:p.Phe314=
ENST00000264468.9:c.780T=	ENSP00000264468.6:p.Phe260=
ENST00000330540.6:c.942T=	ENSP00000332049.2:p.Phe314=
ENST00000393627.6:c.924T=	ENSP00000377248.2:p.Phe308=
ENST00000469710.5:c.696T=	ENSP00000418988.1:p.Phe232=
ENST00000478741.1:c.784T=
ENST00000493101.5:c.606T=	ENSP00000420230.1:p.Phe202=
NM_001206924.1:c.606T=	NP_001193853.1:p.Phe202=
NM_001206925.1:c.696T=	NP_001193854.1:p.Phe232=
NM_006889.4:c.924T=	NP_008820.3:p.Phe308=
NM_175862.4:c.942T=	NP_787058.4:p.Phe314=
NM_176892.1:c.780T=	NP_795711.1:p.Phe260=
NM_175862.5:c.942T= MANE Select	NP_787058.5:p.Phe314=
NM_001206924.2:c.606T=	NP_001193853.2:p.Phe202=
NM_001206925.2:c.696T=	NP_001193854.2:p.Phe232=
NM_006889.5:c.924T=	NP_008820.4:p.Phe308=
NM_176892.2:c.780T=	NP_795711.2:p.Phe260=