Canonical Allele Identifier: CA1618519685

Gene: HLA-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29944624_29944626delinsAGG , CM000668.2:g.29944624_29944626delinsAGG	GRCh38
NC_000006.11:g.29912401_29912403delinsAGG , CM000668.1:g.29912401_29912403delinsAGG	GRCh37
NC_000006.10:g.30020380_30020382delinsAGG	NCBI36
NG_029217.2:g.7160_7162delinsAGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000638375.2:c.895+227_895+229delinsAGG	ENSP00000492789.2:n.895+227_895+229delinsAGG
ENST00000706892.1:n.1976_1978delinsAGG
ENST00000706893.1:c.1054_1056delinsAGG	ENSP00000516609.1:p.Arg352=
ENST00000706894.1:c.1012+8_1012+10delinsAGG	ENSP00000516610.1:n.1012+8_1012+10delinsAGG
ENST00000706895.1:n.1398_1400delinsAGG
ENST00000706896.1:n.1874_1876delinsAGG
ENST00000706897.1:n.1296_1298delinsAGG
ENST00000706898.1:c.1020_1022delinsAGG	ENSP00000516611.1:p.Glu340=
ENST00000706899.1:n.1866+8_1866+10delinsAGG
ENST00000706900.1:c.928+8_928+10delinsAGG	ENSP00000516617.1:n.928+8_928+10delinsAGG
ENST00000706901.1:c.1012+8_1012+10delinsAGG	ENSP00000516612.1:n.1012+8_1012+10delinsAGG
ENST00000706902.1:c.1012+8_1012+10delinsAGG	ENSP00000516613.1:n.1012+8_1012+10delinsAGG
ENST00000706903.1:c.1012+8_1012+10delinsAGG	ENSP00000516614.1:n.1012+8_1012+10delinsAGG
ENST00000706904.1:c.1012+8_1012+10delinsAGG	ENSP00000516615.1:n.1012+8_1012+10delinsAGG
ENST00000706905.1:c.1012+8_1012+10delinsAGG	ENSP00000516616.1:n.1012+8_1012+10delinsAGG
ENST00000376809.10:c.1012+8_1012+10delinsAGG MANE Select	ENSP00000366005.5:n.1012+8_1012+10delinsAGG
ENST00000638375.1:c.895+227_895+229delinsAGG	ENSP00000492789.1:n.895+227_895+229delinsAGG
ENST00000376802.2:c.895+227_895+229delinsAGG	ENSP00000365998.2:n.895+227_895+229delinsAGG
ENST00000376806.9:c.1020_1022delinsAGG	ENSP00000366002.5:p.Glu340=
ENST00000376809.9:c.1012+8_1012+10delinsAGG	ENSP00000366005.5:n.1012+8_1012+10delinsAGG
ENST00000396634.5:c.1012+8_1012+10delinsAGG	ENSP00000379873.1:n.1012+8_1012+10delinsAGG
ENST00000461903.1:n.1261_1263delinsAGG
ENST00000479320.5:n.1253+8_1253+10delinsAGG
ENST00000495183.5:n.1255+8_1255+10delinsAGG
ENST00000496081.5:n.837_839delinsAGG
NM_002116.7:c.1012+8_1012+10delinsAGG	NP_002107.3:n.1012+8_1012+10delinsAGG
NM_002116.8:c.1012+8_1012+10delinsAGG MANE Select	NP_002107.3:n.1012+8_1012+10delinsAGG