Canonical Allele Identifier: CA2677794957

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29944621-A-AAG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29944621_29944622insAG , CM000668.2:g.29944621_29944622insAG	GRCh38
NC_000006.11:g.29912398_29912399insAG , CM000668.1:g.29912398_29912399insAG	GRCh37
NC_000006.10:g.30020377_30020378insAG	NCBI36
NG_029217.2:g.7157_7158insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.895+224_895+225insAG	ENSP00000492789.2:n.895+224_895+225insAG
ENST00000706892.1:n.1973_1974insAG
ENST00000706893.1:c.1051_1052insAG	ENSP00000516609.1:p.Arg351LysfsTer?
ENST00000706894.1:c.1012+5_1012+6insAG	ENSP00000516610.1:n.1012+5_1012+6insAG
ENST00000706895.1:n.1395_1396insAG
ENST00000706896.1:n.1871_1872insAG
ENST00000706897.1:n.1293_1294insAG
ENST00000706898.1:c.1017_1018insAG	ENSP00000516611.1:p.Glu340ArgfsTer4
ENST00000706899.1:n.1866+5_1866+6insAG
ENST00000706900.1:c.928+5_928+6insAG	ENSP00000516617.1:n.928+5_928+6insAG
ENST00000706901.1:c.1012+5_1012+6insAG	ENSP00000516612.1:n.1012+5_1012+6insAG
ENST00000706902.1:c.1012+5_1012+6insAG	ENSP00000516613.1:n.1012+5_1012+6insAG
ENST00000706903.1:c.1012+5_1012+6insAG	ENSP00000516614.1:n.1012+5_1012+6insAG
ENST00000706904.1:c.1012+5_1012+6insAG	ENSP00000516615.1:n.1012+5_1012+6insAG
ENST00000706905.1:c.1012+5_1012+6insAG	ENSP00000516616.1:n.1012+5_1012+6insAG
ENST00000376809.10:c.1012+5_1012+6insAG MANE Select	ENSP00000366005.5:n.1012+5_1012+6insAG
ENST00000638375.1:c.895+224_895+225insAG	ENSP00000492789.1:n.895+224_895+225insAG
ENST00000376802.2:c.895+224_895+225insAG	ENSP00000365998.2:n.895+224_895+225insAG
ENST00000376806.9:c.1017_1018insAG	ENSP00000366002.5:p.Glu340ArgfsTer4
ENST00000376809.9:c.1012+5_1012+6insAG	ENSP00000366005.5:n.1012+5_1012+6insAG
ENST00000396634.5:c.1012+5_1012+6insAG	ENSP00000379873.1:n.1012+5_1012+6insAG
ENST00000461903.1:n.1258_1259insAG
ENST00000479320.5:n.1253+5_1253+6insAG
ENST00000495183.5:n.1255+5_1255+6insAG
ENST00000496081.5:n.834_835insAG
NM_002116.7:c.1012+5_1012+6insAG	NP_002107.3:n.1012+5_1012+6insAG
NM_002116.8:c.1012+5_1012+6insAG MANE Select	NP_002107.3:n.1012+5_1012+6insAG