Canonical Allele Identifier: CA1618520100

Gene: HLA-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29944889_29944891delinsGCT , CM000668.2:g.29944889_29944891delinsGCT	GRCh38
NC_000006.11:g.29912666_29912668delinsGCT , CM000668.1:g.29912666_29912668delinsGCT	GRCh37
NC_000006.10:g.30020645_30020647delinsGCT	NCBI36
NG_029217.2:g.7425_7427delinsGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.896-170_896-168delinsGCT	ENSP00000492789.2:n.896-170_896-168delinsGCT
ENST00000706892.1:n.2241_2243delinsGCT
ENST00000706893.1:c.1065-170_1065-168delinsGCT	ENSP00000516609.1:n.1065-170_1065-168delinsGCT
ENST00000706894.1:c.1013-170_1013-168delinsGCT	ENSP00000516610.1:n.1013-170_1013-168delinsGCT
ENST00000706895.1:n.1663_1665delinsGCT
ENST00000706896.1:n.2139_2141delinsGCT
ENST00000706897.1:n.1561_1563delinsGCT
ENST00000706898.1:c.1031-170_1031-168delinsGCT	ENSP00000516611.1:n.1031-170_1031-168delinsGCT
ENST00000706899.1:n.1867-170_1867-168delinsGCT
ENST00000706900.1:c.929-170_929-168delinsGCT	ENSP00000516617.1:n.929-170_929-168delinsGCT
ENST00000706901.1:c.1013-170_1013-168delinsGCT	ENSP00000516612.1:n.1013-170_1013-168delinsGCT
ENST00000706902.1:c.1013-170_1013-168delinsGCT	ENSP00000516613.1:n.1013-170_1013-168delinsGCT
ENST00000706903.1:c.1013-170_1013-168delinsGCT	ENSP00000516614.1:n.1013-170_1013-168delinsGCT
ENST00000706904.1:c.1013-170_1013-168delinsGCT	ENSP00000516615.1:n.1013-170_1013-168delinsGCT
ENST00000706905.1:c.1013-170_1013-168delinsGCT	ENSP00000516616.1:n.1013-170_1013-168delinsGCT
ENST00000376809.10:c.1013-170_1013-168delinsGCT MANE Select	ENSP00000366005.5:n.1013-170_1013-168delinsGCT
ENST00000638375.1:c.896-170_896-168delinsGCT	ENSP00000492789.1:n.896-170_896-168delinsGCT
ENST00000376802.2:c.895+492_895+494delinsGCT	ENSP00000365998.2:n.895+492_895+494delinsGCT
ENST00000376806.9:c.1031-170_1031-168delinsGCT	ENSP00000366002.5:n.1031-170_1031-168delinsGCT
ENST00000376809.9:c.1013-170_1013-168delinsGCT	ENSP00000366005.5:n.1013-170_1013-168delinsGCT
ENST00000396634.5:c.1013-170_1013-168delinsGCT	ENSP00000379873.1:n.1013-170_1013-168delinsGCT
ENST00000461903.1:n.1272-170_1272-168delinsGCT
ENST00000479320.5:n.1254-170_1254-168delinsGCT
ENST00000495183.5:n.1256-174_1256-172delinsGCT
ENST00000496081.5:n.1102_1104delinsGCT
NM_002116.7:c.1013-170_1013-168delinsGCT	NP_002107.3:n.1013-170_1013-168delinsGCT
NM_002116.8:c.1013-170_1013-168delinsGCT MANE Select	NP_002107.3:n.1013-170_1013-168delinsGCT