Canonical Allele Identifier: CA2677794762

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29944563-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29944566_29944567del , CM000668.2:g.29944566_29944567del	GRCh38
NC_000006.11:g.29912343_29912344del , CM000668.1:g.29912343_29912344del	GRCh37
NC_000006.10:g.30020322_30020323del	NCBI36
NG_029217.2:g.7102_7103del

Transcript Alleles

HGVS	Amino-acid change
ENST00000638375.2:c.895+169_895+170del	ENSP00000492789.2:n.895+169_895+170del
ENST00000706892.1:n.1918_1919del
ENST00000706893.1:c.996_997del	ENSP00000516609.1:p.Cys332Ter
ENST00000706894.1:c.962_963del	ENSP00000516610.1:p.Val321AspfsTer18
ENST00000706895.1:n.1340_1341del
ENST00000706896.1:n.1816_1817del
ENST00000706897.1:n.1238_1239del
ENST00000706898.1:c.962_963del	ENSP00000516611.1:p.Val321AspfsTer24
ENST00000706899.1:n.1816_1817del
ENST00000706900.1:c.878_879del	ENSP00000516617.1:p.Val293AspfsTer18
ENST00000706901.1:c.962_963del	ENSP00000516612.1:p.Val321AspfsTer18
ENST00000706902.1:c.962_963del	ENSP00000516613.1:p.Val321AspfsTer18
ENST00000706903.1:c.962_963del	ENSP00000516614.1:p.Val321AspfsTer18
ENST00000706904.1:c.962_963del	ENSP00000516615.1:p.Val321AspfsTer18
ENST00000706905.1:c.962_963del	ENSP00000516616.1:p.Val321AspfsTer18
ENST00000376809.10:c.962_963del MANE Select	ENSP00000366005.5:p.Val321AspfsTer18
ENST00000638375.1:c.895+169_895+170del	ENSP00000492789.1:n.895+169_895+170del
ENST00000376802.2:c.895+169_895+170del	ENSP00000365998.2:n.895+169_895+170del
ENST00000376806.9:c.962_963del	ENSP00000366002.5:p.Val321AspfsTer24
ENST00000376809.9:c.962_963del	ENSP00000366005.5:p.Val321AspfsTer18
ENST00000396634.5:c.962_963del	ENSP00000379873.1:p.Val321AspfsTer18
ENST00000461903.1:n.1203_1204del
ENST00000479320.5:n.1203_1204del
ENST00000495183.5:n.1205_1206del
ENST00000496081.5:n.779_780del
NM_002116.7:c.962_963del	NP_002107.3:p.Val321AspfsTer18
NM_002116.8:c.962_963del MANE Select	NP_002107.3:p.Val321AspfsTer18