Canonical Allele Identifier: CA2572873785

Gene: CD86

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122066880_122066881del , CM000665.2:g.122066880_122066881del	GRCh38
NC_000003.11:g.121785727_121785728del , CM000665.1:g.121785727_121785728del	GRCh37
NC_000003.10:g.123268417_123268418del	NCBI36
NG_029928.1:g.16519_16520del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330540.7:c.14+11377_14+11378del MANE Select	ENSP00000332049.2:n.14+11377_14+11378del
ENST00000330540.6:c.14+11377_14+11378del	ENSP00000332049.2:n.14+11377_14+11378del
ENST00000469710.5:c.-183+11377_-183+11378del	ENSP00000418988.1:n.-183+11377_-183+11378del
ENST00000478390.1:n.127+11377_127+11378del
ENST00000493101.5:c.14+11377_14+11378del	ENSP00000420230.1:n.14+11377_14+11378del
NM_001206924.1:c.14+11377_14+11378del	NP_001193853.1:n.14+11377_14+11378del
NM_001206925.1:c.-183+11377_-183+11378del	NP_001193854.1:n.-183+11377_-183+11378del
NM_175862.4:c.14+11377_14+11378del	NP_787058.4:n.14+11377_14+11378del
NM_175862.5:c.14+11377_14+11378del MANE Select	NP_787058.5:n.14+11377_14+11378del
NM_001206924.2:c.14+11377_14+11378del	NP_001193853.2:n.14+11377_14+11378del
NM_001206925.2:c.-183+11377_-183+11378del	NP_001193854.2:n.-183+11377_-183+11378del