Canonical Allele Identifier: CA1087349723

Gene: HLA-A

Linked Data

• dbSNP Id: rs1771556123
• gnomAD v3: 6-29945302-ATG-A
• gnomAD v4: 6-29945302-ATG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945308_29945309del , CM000668.2:g.29945308_29945309del	GRCh38
NC_000006.11:g.29913085_29913086del , CM000668.1:g.29913085_29913086del	GRCh37
NC_000006.10:g.30021064_30021065del	NCBI36
NG_029217.2:g.7844_7845del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.976+27_976+28del	ENSP00000492789.2:n.976+27_976+28del
ENST00000706892.1:n.2660_2661del
ENST00000706893.1:c.*77+27_*77+28del	ENSP00000516609.1:n.*77+27_*77+28del
ENST00000706894.1:c.1120_1121del	ENSP00000516610.1:p.Val374TrpfsTer28
ENST00000706895.1:n.1940_1941del
ENST00000706896.1:n.2389+27_2389+28del
ENST00000706897.1:n.1811+27_1811+28del
ENST00000706898.1:c.1111+27_1111+28del	ENSP00000516611.1:n.1111+27_1111+28del
ENST00000706899.1:n.1947+27_1947+28del
ENST00000706900.1:c.1009+27_1009+28del	ENSP00000516617.1:n.1009+27_1009+28del
ENST00000706901.1:c.1093+27_1093+28del	ENSP00000516612.1:n.1093+27_1093+28del
ENST00000706902.1:c.1093+27_1093+28del	ENSP00000516613.1:n.1093+27_1093+28del
ENST00000706903.1:c.1093+27_1093+28del	ENSP00000516614.1:n.1093+27_1093+28del
ENST00000706904.1:c.1093+27_1093+28del	ENSP00000516615.1:n.1093+27_1093+28del
ENST00000706905.1:c.1093+27_1093+28del	ENSP00000516616.1:n.1093+27_1093+28del
ENST00000376809.10:c.1093+27_1093+28del MANE Select	ENSP00000366005.5:n.1093+27_1093+28del
ENST00000376802.2:c.896-143_896-142del	ENSP00000365998.2:n.896-143_896-142del
ENST00000376806.9:c.1111+27_1111+28del	ENSP00000366002.5:n.1111+27_1111+28del
ENST00000376809.9:c.1093+27_1093+28del	ENSP00000366005.5:n.1093+27_1093+28del
ENST00000396634.5:c.1093+27_1093+28del	ENSP00000379873.1:n.1093+27_1093+28del
ENST00000495183.5:n.1332+27_1332+28del
ENST00000496081.5:n.1352+27_1352+28del
NM_002116.7:c.1093+27_1093+28del	NP_002107.3:n.1093+27_1093+28del
NM_002116.8:c.1093+27_1093+28del MANE Select	NP_002107.3:n.1093+27_1093+28del