Canonical Allele Identifier: CA1397810412

Gene: CD86

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122119177G= , CM000665.2:g.122119177G=	GRCh38
NC_000003.11:g.121838024G= , CM000665.1:g.121838024G=	GRCh37
NC_000003.10:g.123320714G=	NCBI36
NG_029928.1:g.68816G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330540.7:c.894-261G= MANE Select	ENSP00000332049.2:n.894-261G=
ENST00000264468.9:c.732-261G=	ENSP00000264468.6:n.732-261G=
ENST00000330540.6:c.894-261G=	ENSP00000332049.2:n.894-261G=
ENST00000393627.6:c.876-261G=	ENSP00000377248.2:n.876-261G=
ENST00000469710.5:c.648-261G=	ENSP00000418988.1:n.648-261G=
ENST00000478741.1:c.736-261G=
ENST00000493101.5:c.558-261G=	ENSP00000420230.1:n.558-261G=
NM_001206924.1:c.558-261G=	NP_001193853.1:n.558-261G=
NM_001206925.1:c.648-261G=	NP_001193854.1:n.648-261G=
NM_006889.4:c.876-261G=	NP_008820.3:n.876-261G=
NM_175862.4:c.894-261G=	NP_787058.4:n.894-261G=
NM_176892.1:c.732-261G=	NP_795711.1:n.732-261G=
NM_175862.5:c.894-261G= MANE Select	NP_787058.5:n.894-261G=
NM_001206924.2:c.558-261G=	NP_001193853.2:n.558-261G=
NM_001206925.2:c.648-261G=	NP_001193854.2:n.648-261G=
NM_006889.5:c.876-261G=	NP_008820.4:n.876-261G=
NM_176892.2:c.732-261G=	NP_795711.2:n.732-261G=