Canonical Allele Identifier: CA2840060563

Gene: HLA-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29943308_29943317del , CM000668.2:g.29943308_29943317del	GRCh38
NC_000006.11:g.29911085_29911094del , CM000668.1:g.29911085_29911094del	GRCh37
NC_000006.10:g.30019064_30019073del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.384_393del	ENSP00000492789.2:p.Ser129AlafsTer19
ENST00000706892.1:n.660_669del
ENST00000706893.1:c.384_393del	ENSP00000516609.1:p.Ser129AlafsTer19
ENST00000706894.1:c.384_393del	ENSP00000516610.1:p.Ser129AlafsTer19
ENST00000706895.1:n.660_669del
ENST00000706896.1:n.660_669del
ENST00000706897.1:n.660_669del
ENST00000706898.1:c.384_393del	ENSP00000516611.1:p.Ser129AlafsTer19
ENST00000706899.1:n.660_669del
ENST00000706900.1:c.300_309del	ENSP00000516617.1:p.Ser101AlafsTer19
ENST00000706901.1:c.384_393del	ENSP00000516612.1:p.Ser129AlafsTer19
ENST00000706902.1:c.384_393del	ENSP00000516613.1:p.Ser129AlafsTer19
ENST00000706903.1:c.384_393del	ENSP00000516614.1:p.Ser129AlafsTer19
ENST00000706904.1:c.384_393del	ENSP00000516615.1:p.Ser129AlafsTer19
ENST00000706905.1:c.384_393del	ENSP00000516616.1:p.Ser129AlafsTer19
ENST00000376809.10:c.384_393del MANE Select	ENSP00000366005.5:p.Ser129AlafsTer19
ENST00000638375.1:c.384_393del	ENSP00000492789.1:p.Ser129AlafsTer19
ENST00000376802.2:c.384_393del	ENSP00000365998.2:p.Ser129AlafsTer19
ENST00000376806.9:c.384_393del	ENSP00000366002.5:p.Ser129AlafsTer19
ENST00000376809.9:c.384_393del	ENSP00000366005.5:p.Ser129AlafsTer19
ENST00000396634.5:c.384_393del	ENSP00000379873.1:p.Ser129AlafsTer19
ENST00000461903.1:n.625_634del
ENST00000479320.5:n.625_634del
ENST00000495183.5:n.627_636del
ENST00000496081.5:n.201_210del
NM_002116.7:c.384_393del	NP_002107.3:p.Ser129AlafsTer19
NM_002116.8:c.384_393del MANE Select	NP_002107.3:p.Ser129AlafsTer19