Canonical Allele Identifier: CA2770463998

Gene: HLA-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945324_29945327del , CM000668.2:g.29945324_29945327del	GRCh38
NC_000006.11:g.29913101_29913104del , CM000668.1:g.29913101_29913104del	GRCh37
NC_000006.10:g.30021080_30021083del	NCBI36
NG_029217.2:g.7860_7863del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.976+43_976+46del	ENSP00000492789.2:n.976+43_976+46del
ENST00000706892.1:n.2676_2679del
ENST00000706893.1:c.*77+43_*77+46del	ENSP00000516609.1:n.*77+43_*77+46del
ENST00000706894.1:c.1136_1139del	ENSP00000516610.1:p.Glu379GlyfsTer29
ENST00000706895.1:n.1956_1959del
ENST00000706896.1:n.2389+43_2389+46del
ENST00000706897.1:n.1811+43_1811+46del
ENST00000706898.1:c.1111+43_1111+46del	ENSP00000516611.1:n.1111+43_1111+46del
ENST00000706899.1:n.1947+43_1947+46del
ENST00000706900.1:c.1009+43_1009+46del	ENSP00000516617.1:n.1009+43_1009+46del
ENST00000706901.1:c.1093+43_1093+46del	ENSP00000516612.1:n.1093+43_1093+46del
ENST00000706902.1:c.1093+43_1093+46del	ENSP00000516613.1:n.1093+43_1093+46del
ENST00000706903.1:c.1093+43_1093+46del	ENSP00000516614.1:n.1093+43_1093+46del
ENST00000706904.1:c.1093+43_1093+46del	ENSP00000516615.1:n.1093+43_1093+46del
ENST00000706905.1:c.1093+43_1093+46del	ENSP00000516616.1:n.1093+43_1093+46del
ENST00000376809.10:c.1093+43_1093+46del MANE Select	ENSP00000366005.5:n.1093+43_1093+46del
ENST00000376802.2:c.896-127_896-124del	ENSP00000365998.2:n.896-127_896-124del
ENST00000376806.9:c.1111+43_1111+46del	ENSP00000366002.5:n.1111+43_1111+46del
ENST00000376809.9:c.1093+43_1093+46del	ENSP00000366005.5:n.1093+43_1093+46del
ENST00000396634.5:c.1093+43_1093+46del	ENSP00000379873.1:n.1093+43_1093+46del
ENST00000495183.5:n.1332+43_1332+46del
ENST00000496081.5:n.1352+43_1352+46del
NM_002116.7:c.1093+43_1093+46del	NP_002107.3:n.1093+43_1093+46del
NM_002116.8:c.1093+43_1093+46del MANE Select	NP_002107.3:n.1093+43_1093+46del