Canonical Allele Identifier: CA1397810634

Gene: CD86

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122119442A= , CM000665.2:g.122119442A=	GRCh38
NC_000003.11:g.121838289A= , CM000665.1:g.121838289A=	GRCh37
NC_000003.10:g.123320979A=	NCBI36
NG_029928.1:g.69081A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000330540.7:c.898A= MANE Select	ENSP00000332049.2:p.Lys300=
ENST00000264468.9:c.736A=	ENSP00000264468.6:p.Lys246=
ENST00000330540.6:c.898A=	ENSP00000332049.2:p.Lys300=
ENST00000393627.6:c.880A=	ENSP00000377248.2:p.Lys294=
ENST00000469710.5:c.652A=	ENSP00000418988.1:p.Lys218=
ENST00000478741.1:c.740A=
ENST00000493101.5:c.562A=	ENSP00000420230.1:p.Lys188=
NM_001206924.1:c.562A=	NP_001193853.1:p.Lys188=
NM_001206925.1:c.652A=	NP_001193854.1:p.Lys218=
NM_006889.4:c.880A=	NP_008820.3:p.Lys294=
NM_175862.4:c.898A=	NP_787058.4:p.Lys300=
NM_176892.1:c.736A=	NP_795711.1:p.Lys246=
NM_175862.5:c.898A= MANE Select	NP_787058.5:p.Lys300=
NM_001206924.2:c.562A=	NP_001193853.2:p.Lys188=
NM_001206925.2:c.652A=	NP_001193854.2:p.Lys218=
NM_006889.5:c.880A=	NP_008820.4:p.Lys294=
NM_176892.2:c.736A=	NP_795711.2:p.Lys246=