Canonical Allele Identifier: CA354163889

Gene: CD86

Linked Data

• MyVariant Identifiers: chr3:g.121838340T>G (hg19) ; chr3:g.122119493T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122119493T>G , CM000665.2:g.122119493T>G	GRCh38
NC_000003.11:g.121838340T>G , CM000665.1:g.121838340T>G	GRCh37
NC_000003.10:g.123321030T>G	NCBI36
NG_029928.1:g.69132T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330540.7:c.949T>G MANE Select	ENSP00000332049.2:p.Ser317Ala
ENST00000264468.9:c.787T>G	ENSP00000264468.6:p.Ser263Ala
ENST00000330540.6:c.949T>G	ENSP00000332049.2:p.Ser317Ala
ENST00000393627.6:c.931T>G	ENSP00000377248.2:p.Ser311Ala
ENST00000469710.5:c.703T>G	ENSP00000418988.1:p.Ser235Ala
ENST00000478741.1:c.791T>G
ENST00000493101.5:c.613T>G	ENSP00000420230.1:p.Ser205Ala
NM_001206924.1:c.613T>G	NP_001193853.1:p.Ser205Ala
NM_001206925.1:c.703T>G	NP_001193854.1:p.Ser235Ala
NM_006889.4:c.931T>G	NP_008820.3:p.Ser311Ala
NM_175862.4:c.949T>G	NP_787058.4:p.Ser317Ala
NM_176892.1:c.787T>G	NP_795711.1:p.Ser263Ala
NM_175862.5:c.949T>G MANE Select	NP_787058.5:p.Ser317Ala
NM_001206924.2:c.613T>G	NP_001193853.2:p.Ser205Ala
NM_001206925.2:c.703T>G	NP_001193854.2:p.Ser235Ala
NM_006889.5:c.931T>G	NP_008820.4:p.Ser311Ala
NM_176892.2:c.787T>G	NP_795711.2:p.Ser263Ala