Canonical Allele Identifier: CA1397810714

Gene: CD86

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122119494C= , CM000665.2:g.122119494C=	GRCh38
NC_000003.11:g.121838341C= , CM000665.1:g.121838341C=	GRCh37
NC_000003.10:g.123321031C=	NCBI36
NG_029928.1:g.69133C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330540.7:c.950C= MANE Select	ENSP00000332049.2:p.Ser317=
ENST00000264468.9:c.788C=	ENSP00000264468.6:p.Ser263=
ENST00000330540.6:c.950C=	ENSP00000332049.2:p.Ser317=
ENST00000393627.6:c.932C=	ENSP00000377248.2:p.Ser311=
ENST00000469710.5:c.704C=	ENSP00000418988.1:p.Ser235=
ENST00000478741.1:c.792C=
ENST00000493101.5:c.614C=	ENSP00000420230.1:p.Ser205=
NM_001206924.1:c.614C=	NP_001193853.1:p.Ser205=
NM_001206925.1:c.704C=	NP_001193854.1:p.Ser235=
NM_006889.4:c.932C=	NP_008820.3:p.Ser311=
NM_175862.4:c.950C=	NP_787058.4:p.Ser317=
NM_176892.1:c.788C=	NP_795711.1:p.Ser263=
NM_175862.5:c.950C= MANE Select	NP_787058.5:p.Ser317=
NM_001206924.2:c.614C=	NP_001193853.2:p.Ser205=
NM_001206925.2:c.704C=	NP_001193854.2:p.Ser235=
NM_006889.5:c.932C=	NP_008820.4:p.Ser311=
NM_176892.2:c.788C=	NP_795711.2:p.Ser263=