Canonical Allele Identifier: CA1618519232

Gene: HLA-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29944385_29944386delinsAC , CM000668.2:g.29944385_29944386delinsAC	GRCh38
NC_000006.11:g.29912162_29912163delinsAC , CM000668.1:g.29912162_29912163delinsAC	GRCh37
NC_000006.10:g.30020141_30020142delinsAC	NCBI36
NG_029217.2:g.6921_6922delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.883_884delinsAC	ENSP00000492789.2:p.Thr295=
ENST00000706892.1:n.1737_1738delinsAC
ENST00000706893.1:c.883_884delinsAC	ENSP00000516609.1:p.Thr295=
ENST00000706894.1:c.883_884delinsAC	ENSP00000516610.1:p.Thr295=
ENST00000706895.1:n.1159_1160delinsAC
ENST00000706896.1:n.1737_1738delinsAC
ENST00000706897.1:n.1159_1160delinsAC
ENST00000706898.1:c.883_884delinsAC	ENSP00000516611.1:p.Thr295=
ENST00000706899.1:n.1737_1738delinsAC
ENST00000706900.1:c.799_800delinsAC	ENSP00000516617.1:p.Thr267=
ENST00000706901.1:c.883_884delinsAC	ENSP00000516612.1:p.Thr295=
ENST00000706902.1:c.883_884delinsAC	ENSP00000516613.1:p.Thr295=
ENST00000706903.1:c.883_884delinsAC	ENSP00000516614.1:p.Thr295=
ENST00000706904.1:c.883_884delinsAC	ENSP00000516615.1:p.Thr295=
ENST00000706905.1:c.883_884delinsAC	ENSP00000516616.1:p.Thr295=
ENST00000376809.10:c.883_884delinsAC MANE Select	ENSP00000366005.5:p.Thr295=
ENST00000638375.1:c.883_884delinsAC	ENSP00000492789.1:p.Thr295=
ENST00000376802.2:c.883_884delinsAC	ENSP00000365998.2:p.Thr295=
ENST00000376806.9:c.883_884delinsAC	ENSP00000366002.5:p.Thr295=
ENST00000376809.9:c.883_884delinsAC	ENSP00000366005.5:p.Thr295=
ENST00000396634.5:c.883_884delinsAC	ENSP00000379873.1:p.Thr295=
ENST00000461903.1:n.1124_1125delinsAC
ENST00000479320.5:n.1124_1125delinsAC
ENST00000495183.5:n.1126_1127delinsAC
ENST00000496081.5:n.700_701delinsAC
NM_002116.7:c.883_884delinsAC	NP_002107.3:p.Thr295=
NM_002116.8:c.883_884delinsAC MANE Select	NP_002107.3:p.Thr295=