Canonical Allele Identifier: CA1618519726

Gene: HLA-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29944639_29944641delinsGGT , CM000668.2:g.29944639_29944641delinsGGT	GRCh38
NC_000006.11:g.29912416_29912418delinsGGT , CM000668.1:g.29912416_29912418delinsGGT	GRCh37
NC_000006.10:g.30020395_30020397delinsGGT	NCBI36
NG_029217.2:g.7175_7177delinsGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.895+242_895+244delinsGGT	ENSP00000492789.2:n.895+242_895+244delinsGGT
ENST00000706892.1:n.1991_1993delinsGGT
ENST00000706893.1:c.1064+5_1064+7delinsGGT	ENSP00000516609.1:n.1064+5_1064+7delinsGGT
ENST00000706894.1:c.1012+23_1012+25delinsGGT	ENSP00000516610.1:n.1012+23_1012+25delinsGGT
ENST00000706895.1:n.1413_1415delinsGGT
ENST00000706896.1:n.1889_1891delinsGGT
ENST00000706897.1:n.1311_1313delinsGGT
ENST00000706898.1:c.1030+5_1030+7delinsGGT	ENSP00000516611.1:n.1030+5_1030+7delinsGGT
ENST00000706899.1:n.1866+23_1866+25delinsGGT
ENST00000706900.1:c.928+23_928+25delinsGGT	ENSP00000516617.1:n.928+23_928+25delinsGGT
ENST00000706901.1:c.1012+23_1012+25delinsGGT	ENSP00000516612.1:n.1012+23_1012+25delinsGGT
ENST00000706902.1:c.1012+23_1012+25delinsGGT	ENSP00000516613.1:n.1012+23_1012+25delinsGGT
ENST00000706903.1:c.1012+23_1012+25delinsGGT	ENSP00000516614.1:n.1012+23_1012+25delinsGGT
ENST00000706904.1:c.1012+23_1012+25delinsGGT	ENSP00000516615.1:n.1012+23_1012+25delinsGGT
ENST00000706905.1:c.1012+23_1012+25delinsGGT	ENSP00000516616.1:n.1012+23_1012+25delinsGGT
ENST00000376809.10:c.1012+23_1012+25delinsGGT MANE Select	ENSP00000366005.5:n.1012+23_1012+25delinsGGT
ENST00000638375.1:c.895+242_895+244delinsGGT	ENSP00000492789.1:n.895+242_895+244delinsGGT
ENST00000376802.2:c.895+242_895+244delinsGGT	ENSP00000365998.2:n.895+242_895+244delinsGGT
ENST00000376806.9:c.1030+5_1030+7delinsGGT	ENSP00000366002.5:n.1030+5_1030+7delinsGGT
ENST00000376809.9:c.1012+23_1012+25delinsGGT	ENSP00000366005.5:n.1012+23_1012+25delinsGGT
ENST00000396634.5:c.1012+23_1012+25delinsGGT	ENSP00000379873.1:n.1012+23_1012+25delinsGGT
ENST00000461903.1:n.1271+5_1271+7delinsGGT
ENST00000479320.5:n.1253+23_1253+25delinsGGT
ENST00000495183.5:n.1255+23_1255+25delinsGGT
ENST00000496081.5:n.852_854delinsGGT
NM_002116.7:c.1012+23_1012+25delinsGGT	NP_002107.3:n.1012+23_1012+25delinsGGT
NM_002116.8:c.1012+23_1012+25delinsGGT MANE Select	NP_002107.3:n.1012+23_1012+25delinsGGT