Canonical Allele Identifier: CA1618519705

Gene: HLA-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29944635_29944636delinsGT , CM000668.2:g.29944635_29944636delinsGT	GRCh38
NC_000006.11:g.29912412_29912413delinsGT , CM000668.1:g.29912412_29912413delinsGT	GRCh37
NC_000006.10:g.30020391_30020392delinsGT	NCBI36
NG_029217.2:g.7171_7172delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.895+238_895+239delinsGT	ENSP00000492789.2:n.895+238_895+239delinsGT
ENST00000706892.1:n.1987_1988delinsGT
ENST00000706893.1:c.1064+1_1064+2delinsGT	ENSP00000516609.1:n.1064+1_1064+2delinsGT
ENST00000706894.1:c.1012+19_1012+20delinsGT	ENSP00000516610.1:n.1012+19_1012+20delinsGT
ENST00000706895.1:n.1409_1410delinsGT
ENST00000706896.1:n.1885_1886delinsGT
ENST00000706897.1:n.1307_1308delinsGT
ENST00000706898.1:c.1030+1_1030+2delinsGT	ENSP00000516611.1:n.1030+1_1030+2delinsGT
ENST00000706899.1:n.1866+19_1866+20delinsGT
ENST00000706900.1:c.928+19_928+20delinsGT	ENSP00000516617.1:n.928+19_928+20delinsGT
ENST00000706901.1:c.1012+19_1012+20delinsGT	ENSP00000516612.1:n.1012+19_1012+20delinsGT
ENST00000706902.1:c.1012+19_1012+20delinsGT	ENSP00000516613.1:n.1012+19_1012+20delinsGT
ENST00000706903.1:c.1012+19_1012+20delinsGT	ENSP00000516614.1:n.1012+19_1012+20delinsGT
ENST00000706904.1:c.1012+19_1012+20delinsGT	ENSP00000516615.1:n.1012+19_1012+20delinsGT
ENST00000706905.1:c.1012+19_1012+20delinsGT	ENSP00000516616.1:n.1012+19_1012+20delinsGT
ENST00000376809.10:c.1012+19_1012+20delinsGT MANE Select	ENSP00000366005.5:n.1012+19_1012+20delinsGT
ENST00000638375.1:c.895+238_895+239delinsGT	ENSP00000492789.1:n.895+238_895+239delinsGT
ENST00000376802.2:c.895+238_895+239delinsGT	ENSP00000365998.2:n.895+238_895+239delinsGT
ENST00000376806.9:c.1030+1_1030+2delinsGT	ENSP00000366002.5:n.1030+1_1030+2delinsGT
ENST00000376809.9:c.1012+19_1012+20delinsGT	ENSP00000366005.5:n.1012+19_1012+20delinsGT
ENST00000396634.5:c.1012+19_1012+20delinsGT	ENSP00000379873.1:n.1012+19_1012+20delinsGT
ENST00000461903.1:n.1271+1_1271+2delinsGT
ENST00000479320.5:n.1253+19_1253+20delinsGT
ENST00000495183.5:n.1255+19_1255+20delinsGT
ENST00000496081.5:n.848_849delinsGT
NM_002116.7:c.1012+19_1012+20delinsGT	NP_002107.3:n.1012+19_1012+20delinsGT
NM_002116.8:c.1012+19_1012+20delinsGT MANE Select	NP_002107.3:n.1012+19_1012+20delinsGT