Canonical Allele Identifier: CA354163846

Gene: CD86

Linked Data

• gnomAD v4: 3-122119473-C-A
• MyVariant Identifiers: chr3:g.121838320C>A (hg19) ; chr3:g.122119473C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122119473C>A , CM000665.2:g.122119473C>A	GRCh38
NC_000003.11:g.121838320C>A , CM000665.1:g.121838320C>A	GRCh37
NC_000003.10:g.123321010C>A	NCBI36
NG_029928.1:g.69112C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000330540.7:c.929C>A MANE Select	ENSP00000332049.2:p.Ala310Asp
ENST00000264468.9:c.767C>A	ENSP00000264468.6:p.Ala256Asp
ENST00000330540.6:c.929C>A	ENSP00000332049.2:p.Ala310Asp
ENST00000393627.6:c.911C>A	ENSP00000377248.2:p.Ala304Asp
ENST00000469710.5:c.683C>A	ENSP00000418988.1:p.Ala228Asp
ENST00000478741.1:c.771C>A
ENST00000493101.5:c.593C>A	ENSP00000420230.1:p.Ala198Asp
NM_001206924.1:c.593C>A	NP_001193853.1:p.Ala198Asp
NM_001206925.1:c.683C>A	NP_001193854.1:p.Ala228Asp
NM_006889.4:c.911C>A	NP_008820.3:p.Ala304Asp
NM_175862.4:c.929C>A	NP_787058.4:p.Ala310Asp
NM_176892.1:c.767C>A	NP_795711.1:p.Ala256Asp
NM_175862.5:c.929C>A MANE Select	NP_787058.5:p.Ala310Asp
NM_001206924.2:c.593C>A	NP_001193853.2:p.Ala198Asp
NM_001206925.2:c.683C>A	NP_001193854.2:p.Ala228Asp
NM_006889.5:c.911C>A	NP_008820.4:p.Ala304Asp
NM_176892.2:c.767C>A	NP_795711.2:p.Ala256Asp