Canonical Allele Identifier: CA1397784397

Gene: CD86

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122066867_122066871delinsAAAAT , CM000665.2:g.122066867_122066871delinsAAAAT	GRCh38
NC_000003.11:g.121785714_121785718delinsAAAAT , CM000665.1:g.121785714_121785718delinsAAAAT	GRCh37
NC_000003.10:g.123268404_123268408delinsAAAAT	NCBI36
NG_029928.1:g.16506_16510delinsAAAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330540.7:c.14+11364_14+11368delinsAAAAT MANE Select	ENSP00000332049.2:n.14+11364_14+11368delinsAAAAT
ENST00000330540.6:c.14+11364_14+11368delinsAAAAT	ENSP00000332049.2:n.14+11364_14+11368delinsAAAAT
ENST00000469710.5:c.-183+11364_-183+11368delinsAAAAT	ENSP00000418988.1:n.-183+11364_-183+11368delinsAAAAT
ENST00000478390.1:n.127+11364_127+11368delinsAAAAT
ENST00000493101.5:c.14+11364_14+11368delinsAAAAT	ENSP00000420230.1:n.14+11364_14+11368delinsAAAAT
NM_001206924.1:c.14+11364_14+11368delinsAAAAT	NP_001193853.1:n.14+11364_14+11368delinsAAAAT
NM_001206925.1:c.-183+11364_-183+11368delinsAAAAT	NP_001193854.1:n.-183+11364_-183+11368delinsAAAAT
NM_175862.4:c.14+11364_14+11368delinsAAAAT	NP_787058.4:n.14+11364_14+11368delinsAAAAT
NM_175862.5:c.14+11364_14+11368delinsAAAAT MANE Select	NP_787058.5:n.14+11364_14+11368delinsAAAAT
NM_001206924.2:c.14+11364_14+11368delinsAAAAT	NP_001193853.2:n.14+11364_14+11368delinsAAAAT
NM_001206925.2:c.-183+11364_-183+11368delinsAAAAT	NP_001193854.2:n.-183+11364_-183+11368delinsAAAAT