Canonical Allele Identifier: CA2677798689

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29945811-GTTAA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945816_29945819del , CM000668.2:g.29945816_29945819del	GRCh38
NC_000006.11:g.29913593_29913596del , CM000668.1:g.29913593_29913596del	GRCh37
NC_000006.10:g.30021572_30021575del	NCBI36
NG_029217.2:g.8352_8355del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.1342_1345del	ENSP00000492789.2:n.1342_1345del
ENST00000706896.1:n.2755_2758del
ENST00000706897.1:n.2177_2180del
ENST00000706898.1:c.*361_*364del	ENSP00000516611.1:n.*361_*364del
ENST00000706899.1:n.2313_2316del
ENST00000706900.1:c.*361_*364del	ENSP00000516617.1:n.*361_*364del
ENST00000706901.1:c.*361_*364del	ENSP00000516612.1:n.*361_*364del
ENST00000706902.1:c.1093+535_1093+538del	ENSP00000516613.1:n.1093+535_1093+538del
ENST00000706903.1:c.*124+237_*124+240del	ENSP00000516614.1:n.*124+237_*124+240del
ENST00000706904.1:c.1093+535_1093+538del	ENSP00000516615.1:n.1093+535_1093+538del
ENST00000706905.1:c.*361_*364del	ENSP00000516616.1:n.*361_*364del
ENST00000376809.10:c.*361_*364del MANE Select	ENSP00000366005.5:n.*361_*364del
ENST00000376802.2:c.*361_*364del	ENSP00000365998.2:n.*361_*364del
ENST00000376806.9:c.*361_*364del	ENSP00000366002.5:n.*361_*364del
ENST00000376809.9:c.*361_*364del	ENSP00000366005.5:n.*361_*364del
ENST00000396634.5:c.*361_*364del	ENSP00000379873.1:n.*361_*364del
ENST00000495183.5:n.1698_1701del
ENST00000496081.5:n.1718_1721del
NM_002116.7:c.*361_*364del	NP_002107.3:n.*361_*364del
NM_002116.8:c.*361_*364del MANE Select	NP_002107.3:n.*361_*364del