Canonical Allele Identifier: CA354163773

Gene: CD86

Linked Data

• MyVariant Identifiers: chr3:g.121838286G>T (hg19) ; chr3:g.122119439G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122119439G>T , CM000665.2:g.122119439G>T	GRCh38
NC_000003.11:g.121838286G>T , CM000665.1:g.121838286G>T	GRCh37
NC_000003.10:g.123320976G>T	NCBI36
NG_029928.1:g.69078G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000330540.7:c.895G>T MANE Select	ENSP00000332049.2:p.Glu299Ter
ENST00000264468.9:c.733G>T	ENSP00000264468.6:p.Glu245Ter
ENST00000330540.6:c.895G>T	ENSP00000332049.2:p.Glu299Ter
ENST00000393627.6:c.877G>T	ENSP00000377248.2:p.Glu293Ter
ENST00000469710.5:c.649G>T	ENSP00000418988.1:p.Glu217Ter
ENST00000478741.1:c.737G>T
ENST00000493101.5:c.559G>T	ENSP00000420230.1:p.Glu187Ter
NM_001206924.1:c.559G>T	NP_001193853.1:p.Glu187Ter
NM_001206925.1:c.649G>T	NP_001193854.1:p.Glu217Ter
NM_006889.4:c.877G>T	NP_008820.3:p.Glu293Ter
NM_175862.4:c.895G>T	NP_787058.4:p.Glu299Ter
NM_176892.1:c.733G>T	NP_795711.1:p.Glu245Ter
NM_175862.5:c.895G>T MANE Select	NP_787058.5:p.Glu299Ter
NM_001206924.2:c.559G>T	NP_001193853.2:p.Glu187Ter
NM_001206925.2:c.649G>T	NP_001193854.2:p.Glu217Ter
NM_006889.5:c.877G>T	NP_008820.4:p.Glu293Ter
NM_176892.2:c.733G>T	NP_795711.2:p.Glu245Ter