Canonical Allele Identifier: CA354163867

Gene: CD86

Linked Data

• MyVariant Identifiers: chr3:g.121838331T>C (hg19) ; chr3:g.122119484T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122119484T>C , CM000665.2:g.122119484T>C	GRCh38
NC_000003.11:g.121838331T>C , CM000665.1:g.121838331T>C	GRCh37
NC_000003.10:g.123321021T>C	NCBI36
NG_029928.1:g.69123T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000330540.7:c.940T>C MANE Select	ENSP00000332049.2:p.Phe314Leu
ENST00000264468.9:c.778T>C	ENSP00000264468.6:p.Phe260Leu
ENST00000330540.6:c.940T>C	ENSP00000332049.2:p.Phe314Leu
ENST00000393627.6:c.922T>C	ENSP00000377248.2:p.Phe308Leu
ENST00000469710.5:c.694T>C	ENSP00000418988.1:p.Phe232Leu
ENST00000478741.1:c.782T>C
ENST00000493101.5:c.604T>C	ENSP00000420230.1:p.Phe202Leu
NM_001206924.1:c.604T>C	NP_001193853.1:p.Phe202Leu
NM_001206925.1:c.694T>C	NP_001193854.1:p.Phe232Leu
NM_006889.4:c.922T>C	NP_008820.3:p.Phe308Leu
NM_175862.4:c.940T>C	NP_787058.4:p.Phe314Leu
NM_176892.1:c.778T>C	NP_795711.1:p.Phe260Leu
NM_175862.5:c.940T>C MANE Select	NP_787058.5:p.Phe314Leu
NM_001206924.2:c.604T>C	NP_001193853.2:p.Phe202Leu
NM_001206925.2:c.694T>C	NP_001193854.2:p.Phe232Leu
NM_006889.5:c.922T>C	NP_008820.4:p.Phe308Leu
NM_176892.2:c.778T>C	NP_795711.2:p.Phe260Leu