Canonical Allele Identifier: CA354163779
Gene: CD86 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122119442A>T , CM000665.2:g.122119442A>T GRCh38
NC_000003.11:g.121838289A>T , CM000665.1:g.121838289A>T GRCh37
NC_000003.10:g.123320979A>T NCBI36
NG_029928.1:g.69081A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000330540.7:c.898A>T MANE Select ENSP00000332049.2:p.Lys300Ter
ENST00000264468.9:c.736A>T ENSP00000264468.6:p.Lys246Ter
ENST00000330540.6:c.898A>T ENSP00000332049.2:p.Lys300Ter
ENST00000393627.6:c.880A>T ENSP00000377248.2:p.Lys294Ter
ENST00000469710.5:c.652A>T ENSP00000418988.1:p.Lys218Ter
ENST00000478741.1:c.740A>T
ENST00000493101.5:c.562A>T ENSP00000420230.1:p.Lys188Ter
NM_001206924.1:c.562A>T NP_001193853.1:p.Lys188Ter
NM_001206925.1:c.652A>T NP_001193854.1:p.Lys218Ter
NM_006889.4:c.880A>T NP_008820.3:p.Lys294Ter
NM_175862.4:c.898A>T NP_787058.4:p.Lys300Ter
NM_176892.1:c.736A>T NP_795711.1:p.Lys246Ter
NM_175862.5:c.898A>T MANE Select NP_787058.5:p.Lys300Ter
NM_001206924.2:c.562A>T NP_001193853.2:p.Lys188Ter
NM_001206925.2:c.652A>T NP_001193854.2:p.Lys218Ter
NM_006889.5:c.880A>T NP_008820.4:p.Lys294Ter
NM_176892.2:c.736A>T NP_795711.2:p.Lys246Ter