Canonical Allele Identifier: CA2667228389

Gene: CD86

Linked Data

• gnomAD v4: 3-122119478-CGT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122119481_122119482del , CM000665.2:g.122119481_122119482del	GRCh38
NC_000003.11:g.121838328_121838329del , CM000665.1:g.121838328_121838329del	GRCh37
NC_000003.10:g.123321018_123321019del	NCBI36
NG_029928.1:g.69120_69121del

Transcript Alleles

HGVS	Amino-acid change
ENST00000330540.7:c.937_938del MANE Select	ENSP00000332049.2:p.Val313PhefsTer2
ENST00000264468.9:c.775_776del	ENSP00000264468.6:p.Val259PhefsTer2
ENST00000330540.6:c.937_938del	ENSP00000332049.2:p.Val313PhefsTer2
ENST00000393627.6:c.919_920del	ENSP00000377248.2:p.Val307PhefsTer2
ENST00000469710.5:c.691_692del	ENSP00000418988.1:p.Val231PhefsTer2
ENST00000478741.1:c.779_780del
ENST00000493101.5:c.601_602del	ENSP00000420230.1:p.Val201PhefsTer2
NM_001206924.1:c.601_602del	NP_001193853.1:p.Val201PhefsTer2
NM_001206925.1:c.691_692del	NP_001193854.1:p.Val231PhefsTer2
NM_006889.4:c.919_920del	NP_008820.3:p.Val307PhefsTer2
NM_175862.4:c.937_938del	NP_787058.4:p.Val313PhefsTer2
NM_176892.1:c.775_776del	NP_795711.1:p.Val259PhefsTer2
NM_175862.5:c.937_938del MANE Select	NP_787058.5:p.Val313PhefsTer2
NM_001206924.2:c.601_602del	NP_001193853.2:p.Val201PhefsTer2
NM_001206925.2:c.691_692del	NP_001193854.2:p.Val231PhefsTer2
NM_006889.5:c.919_920del	NP_008820.4:p.Val307PhefsTer2
NM_176892.2:c.775_776del	NP_795711.2:p.Val259PhefsTer2