Canonical Allele Identifier: CA2535050451
Gene: CD86 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122119274_122119275insTCT , CM000665.2:g.122119274_122119275insTCT GRCh38
NC_000003.11:g.121838121_121838122insTCT , CM000665.1:g.121838121_121838122insTCT GRCh37
NC_000003.10:g.123320811_123320812insTCT NCBI36
NG_029928.1:g.68913_68914insTCT

Transcript Alleles

HGVS Amino-acid change
ENST00000330540.7:c.894-164_894-163insTCT MANE Select ENSP00000332049.2:n.894-164_894-163insTCT
ENST00000264468.9:c.732-164_732-163insTCT ENSP00000264468.6:n.732-164_732-163insTCT
ENST00000330540.6:c.894-164_894-163insTCT ENSP00000332049.2:n.894-164_894-163insTCT
ENST00000393627.6:c.876-164_876-163insTCT ENSP00000377248.2:n.876-164_876-163insTCT
ENST00000469710.5:c.648-164_648-163insTCT ENSP00000418988.1:n.648-164_648-163insTCT
ENST00000478741.1:c.736-164_736-163insTCT
ENST00000493101.5:c.558-164_558-163insTCT ENSP00000420230.1:n.558-164_558-163insTCT
NM_001206924.1:c.558-164_558-163insTCT NP_001193853.1:n.558-164_558-163insTCT
NM_001206925.1:c.648-164_648-163insTCT NP_001193854.1:n.648-164_648-163insTCT
NM_006889.4:c.876-164_876-163insTCT NP_008820.3:n.876-164_876-163insTCT
NM_175862.4:c.894-164_894-163insTCT NP_787058.4:n.894-164_894-163insTCT
NM_176892.1:c.732-164_732-163insTCT NP_795711.1:n.732-164_732-163insTCT
NM_175862.5:c.894-164_894-163insTCT MANE Select NP_787058.5:n.894-164_894-163insTCT
NM_001206924.2:c.558-164_558-163insTCT NP_001193853.2:n.558-164_558-163insTCT
NM_001206925.2:c.648-164_648-163insTCT NP_001193854.2:n.648-164_648-163insTCT
NM_006889.5:c.876-164_876-163insTCT NP_008820.4:n.876-164_876-163insTCT
NM_176892.2:c.732-164_732-163insTCT NP_795711.2:n.732-164_732-163insTCT