Canonical Allele Identifier: CA354163851

Gene: CD86

Linked Data

• MyVariant Identifiers: chr3:g.121838323A>C (hg19) ; chr3:g.122119476A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122119476A>C , CM000665.2:g.122119476A>C	GRCh38
NC_000003.11:g.121838323A>C , CM000665.1:g.121838323A>C	GRCh37
NC_000003.10:g.123321013A>C	NCBI36
NG_029928.1:g.69115A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000330540.7:c.932A>C MANE Select	ENSP00000332049.2:p.Gln311Pro
ENST00000264468.9:c.770A>C	ENSP00000264468.6:p.Gln257Pro
ENST00000330540.6:c.932A>C	ENSP00000332049.2:p.Gln311Pro
ENST00000393627.6:c.914A>C	ENSP00000377248.2:p.Gln305Pro
ENST00000469710.5:c.686A>C	ENSP00000418988.1:p.Gln229Pro
ENST00000478741.1:c.774A>C
ENST00000493101.5:c.596A>C	ENSP00000420230.1:p.Gln199Pro
NM_001206924.1:c.596A>C	NP_001193853.1:p.Gln199Pro
NM_001206925.1:c.686A>C	NP_001193854.1:p.Gln229Pro
NM_006889.4:c.914A>C	NP_008820.3:p.Gln305Pro
NM_175862.4:c.932A>C	NP_787058.4:p.Gln311Pro
NM_176892.1:c.770A>C	NP_795711.1:p.Gln257Pro
NM_175862.5:c.932A>C MANE Select	NP_787058.5:p.Gln311Pro
NM_001206924.2:c.596A>C	NP_001193853.2:p.Gln199Pro
NM_001206925.2:c.686A>C	NP_001193854.2:p.Gln229Pro
NM_006889.5:c.914A>C	NP_008820.4:p.Gln305Pro
NM_176892.2:c.770A>C	NP_795711.2:p.Gln257Pro