Canonical Allele Identifier: CA2770463995

Gene: HLA-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945317_29945329del , CM000668.2:g.29945317_29945329del	GRCh38
NC_000006.11:g.29913094_29913106del , CM000668.1:g.29913094_29913106del	GRCh37
NC_000006.10:g.30021073_30021085del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.976+36_976+48del	ENSP00000492789.2:n.976+36_976+48del
ENST00000706892.1:n.2669_2681del
ENST00000706893.1:c.*77+36_*77+48del	ENSP00000516609.1:n.*77+36_*77+48del
ENST00000706894.1:c.1129_1141del	ENSP00000516610.1:p.Trp377GlyfsTer28
ENST00000706895.1:n.1949_1961del
ENST00000706896.1:n.2389+36_2389+48del
ENST00000706897.1:n.1811+36_1811+48del
ENST00000706898.1:c.1111+36_1111+48del	ENSP00000516611.1:n.1111+36_1111+48del
ENST00000706899.1:n.1947+36_1947+48del
ENST00000706900.1:c.1009+36_1009+48del	ENSP00000516617.1:n.1009+36_1009+48del
ENST00000706901.1:c.1093+36_1093+48del	ENSP00000516612.1:n.1093+36_1093+48del
ENST00000706902.1:c.1093+36_1093+48del	ENSP00000516613.1:n.1093+36_1093+48del
ENST00000706903.1:c.1093+36_1093+48del	ENSP00000516614.1:n.1093+36_1093+48del
ENST00000706904.1:c.1093+36_1093+48del	ENSP00000516615.1:n.1093+36_1093+48del
ENST00000706905.1:c.1093+36_1093+48del	ENSP00000516616.1:n.1093+36_1093+48del
ENST00000376809.10:c.1093+36_1093+48del MANE Select	ENSP00000366005.5:n.1093+36_1093+48del
ENST00000376802.2:c.896-134_896-122del	ENSP00000365998.2:n.896-134_896-122del
ENST00000376806.9:c.1111+36_1111+48del	ENSP00000366002.5:n.1111+36_1111+48del
ENST00000376809.9:c.1093+36_1093+48del	ENSP00000366005.5:n.1093+36_1093+48del
ENST00000396634.5:c.1093+36_1093+48del	ENSP00000379873.1:n.1093+36_1093+48del
ENST00000495183.5:n.1332+36_1332+48del
ENST00000496081.5:n.1352+36_1352+48del
NM_002116.7:c.1093+36_1093+48del	NP_002107.3:n.1093+36_1093+48del
NM_002116.8:c.1093+36_1093+48del MANE Select	NP_002107.3:n.1093+36_1093+48del