Canonical Allele Identifier: CA2677798166

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29945693-GTCTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945694_29945697del , CM000668.2:g.29945694_29945697del	GRCh38
NC_000006.11:g.29913471_29913474del , CM000668.1:g.29913471_29913474del	GRCh37
NC_000006.10:g.30021450_30021453del	NCBI36
NG_029217.2:g.8230_8233del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.1220_1223del	ENSP00000492789.2:n.1220_1223del
ENST00000706892.1:n.3046_3049del
ENST00000706893.1:c.*321_*324del	ENSP00000516609.1:n.*321_*324del
ENST00000706894.1:c.*321_*324del	ENSP00000516610.1:n.*321_*324del
ENST00000706895.1:n.2326_2329del
ENST00000706896.1:n.2633_2636del
ENST00000706897.1:n.2055_2058del
ENST00000706898.1:c.*239_*242del	ENSP00000516611.1:n.*239_*242del
ENST00000706899.1:n.2191_2194del
ENST00000706900.1:c.*239_*242del	ENSP00000516617.1:n.*239_*242del
ENST00000706901.1:c.*239_*242del	ENSP00000516612.1:n.*239_*242del
ENST00000706902.1:c.1093+413_1093+416del	ENSP00000516613.1:n.1093+413_1093+416del
ENST00000706903.1:c.*124+115_*124+118del	ENSP00000516614.1:n.*124+115_*124+118del
ENST00000706904.1:c.1093+413_1093+416del	ENSP00000516615.1:n.1093+413_1093+416del
ENST00000706905.1:c.*239_*242del	ENSP00000516616.1:n.*239_*242del
ENST00000376809.10:c.*239_*242del MANE Select	ENSP00000366005.5:n.*239_*242del
ENST00000376802.2:c.*239_*242del	ENSP00000365998.2:n.*239_*242del
ENST00000376806.9:c.*239_*242del	ENSP00000366002.5:n.*239_*242del
ENST00000376809.9:c.*239_*242del	ENSP00000366005.5:n.*239_*242del
ENST00000396634.5:c.*239_*242del	ENSP00000379873.1:n.*239_*242del
ENST00000495183.5:n.1576_1579del
ENST00000496081.5:n.1596_1599del
NM_002116.7:c.*239_*242del	NP_002107.3:n.*239_*242del
NM_002116.8:c.*239_*242del MANE Select	NP_002107.3:n.*239_*242del