Canonical Allele Identifier: CA2840060559

Gene: HLA-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29943337_29943338insACTGGCGCTTCCTCCGCGGGTACCG , CM000668.2:g.29943337_29943338insACTGGCGCTTCCTCCGCGGGTACCG	GRCh38
NC_000006.11:g.29911114_29911115insACTGGCGCTTCCTCCGCGGGTACCG , CM000668.1:g.29911114_29911115insACTGGCGCTTCCTCCGCGGGTACCG	GRCh37
NC_000006.10:g.30019093_30019094insACTGGCGCTTCCTCCGCGGGTACCG	NCBI36
NG_029217.2:g.5872_5873insACTGGCGCTTCCTCCGCGGGTACCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.413_414insACTGGCGCTTCCTCCGCGGGTACCG	ENSP00000492789.2:p.Gln139LeufsTer?
ENST00000706892.1:n.689_690insACTGGCGCTTCCTCCGCGGGTACCG
ENST00000706893.1:c.413_414insACTGGCGCTTCCTCCGCGGGTACCG	ENSP00000516609.1:p.Gln139LeufsTer?
ENST00000706894.1:c.413_414insACTGGCGCTTCCTCCGCGGGTACCG	ENSP00000516610.1:p.Gln139LeufsTer?
ENST00000706895.1:n.689_690insACTGGCGCTTCCTCCGCGGGTACCG
ENST00000706896.1:n.689_690insACTGGCGCTTCCTCCGCGGGTACCG
ENST00000706897.1:n.689_690insACTGGCGCTTCCTCCGCGGGTACCG
ENST00000706898.1:c.413_414insACTGGCGCTTCCTCCGCGGGTACCG	ENSP00000516611.1:p.Gln139LeufsTer?
ENST00000706899.1:n.689_690insACTGGCGCTTCCTCCGCGGGTACCG
ENST00000706900.1:c.329_330insACTGGCGCTTCCTCCGCGGGTACCG	ENSP00000516617.1:p.Gln111LeufsTer?
ENST00000706901.1:c.413_414insACTGGCGCTTCCTCCGCGGGTACCG	ENSP00000516612.1:p.Gln139LeufsTer?
ENST00000706902.1:c.413_414insACTGGCGCTTCCTCCGCGGGTACCG	ENSP00000516613.1:p.Gln139LeufsTer?
ENST00000706903.1:c.413_414insACTGGCGCTTCCTCCGCGGGTACCG	ENSP00000516614.1:p.Gln139LeufsTer?
ENST00000706904.1:c.413_414insACTGGCGCTTCCTCCGCGGGTACCG	ENSP00000516615.1:p.Gln139LeufsTer?
ENST00000706905.1:c.413_414insACTGGCGCTTCCTCCGCGGGTACCG	ENSP00000516616.1:p.Gln139LeufsTer?
ENST00000376809.10:c.413_414insACTGGCGCTTCCTCCGCGGGTACCG MANE Select	ENSP00000366005.5:p.Gln139LeufsTer?
ENST00000638375.1:c.413_414insACTGGCGCTTCCTCCGCGGGTACCG	ENSP00000492789.1:p.Gln139LeufsTer?
ENST00000376802.2:c.413_414insACTGGCGCTTCCTCCGCGGGTACCG	ENSP00000365998.2:p.Gln139LeufsTer?
ENST00000376806.9:c.413_414insACTGGCGCTTCCTCCGCGGGTACCG	ENSP00000366002.5:p.Gln139LeufsTer?
ENST00000376809.9:c.413_414insACTGGCGCTTCCTCCGCGGGTACCG	ENSP00000366005.5:p.Gln139LeufsTer?
ENST00000396634.5:c.413_414insACTGGCGCTTCCTCCGCGGGTACCG	ENSP00000379873.1:p.Gln139LeufsTer?
ENST00000461903.1:n.654_655insACTGGCGCTTCCTCCGCGGGTACCG
ENST00000479320.5:n.654_655insACTGGCGCTTCCTCCGCGGGTACCG
ENST00000495183.5:n.656_657insACTGGCGCTTCCTCCGCGGGTACCG
ENST00000496081.5:n.230_231insACTGGCGCTTCCTCCGCGGGTACCG
NM_002116.7:c.413_414insACTGGCGCTTCCTCCGCGGGTACCG	NP_002107.3:p.Gln139LeufsTer?
NM_002116.8:c.413_414insACTGGCGCTTCCTCCGCGGGTACCG MANE Select	NP_002107.3:p.Gln139LeufsTer?