Canonical Allele Identifier: CA2677794949

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29944616-G-GGC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29944617_29944618insCG , CM000668.2:g.29944617_29944618insCG	GRCh38
NC_000006.11:g.29912394_29912395insCG , CM000668.1:g.29912394_29912395insCG	GRCh37
NC_000006.10:g.30020373_30020374insCG	NCBI36
NG_029217.2:g.7153_7154insCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.895+220_895+221insCG	ENSP00000492789.2:n.895+220_895+221insCG
ENST00000706892.1:n.1969_1970insCG
ENST00000706893.1:c.1047_1048insCG	ENSP00000516609.1:p.Trp350ArgfsTer?
ENST00000706894.1:c.1012+1_1012+2insCG	ENSP00000516610.1:n.1012+1_1012+2insCG
ENST00000706895.1:n.1391_1392insCG
ENST00000706896.1:n.1867_1868insCG
ENST00000706897.1:n.1289_1290insCG
ENST00000706898.1:c.1013_1014insCG	ENSP00000516611.1:p.Gly339ValfsTer5
ENST00000706899.1:n.1866+1_1866+2insCG
ENST00000706900.1:c.928+1_928+2insCG	ENSP00000516617.1:n.928+1_928+2insCG
ENST00000706901.1:c.1012+1_1012+2insCG	ENSP00000516612.1:n.1012+1_1012+2insCG
ENST00000706902.1:c.1012+1_1012+2insCG	ENSP00000516613.1:n.1012+1_1012+2insCG
ENST00000706903.1:c.1012+1_1012+2insCG	ENSP00000516614.1:n.1012+1_1012+2insCG
ENST00000706904.1:c.1012+1_1012+2insCG	ENSP00000516615.1:n.1012+1_1012+2insCG
ENST00000706905.1:c.1012+1_1012+2insCG	ENSP00000516616.1:n.1012+1_1012+2insCG
ENST00000376809.10:c.1012+1_1012+2insCG MANE Select	ENSP00000366005.5:n.1012+1_1012+2insCG
ENST00000638375.1:c.895+220_895+221insCG	ENSP00000492789.1:n.895+220_895+221insCG
ENST00000376802.2:c.895+220_895+221insCG	ENSP00000365998.2:n.895+220_895+221insCG
ENST00000376806.9:c.1013_1014insCG	ENSP00000366002.5:p.Gly339ValfsTer5
ENST00000376809.9:c.1012+1_1012+2insCG	ENSP00000366005.5:n.1012+1_1012+2insCG
ENST00000396634.5:c.1012+1_1012+2insCG	ENSP00000379873.1:n.1012+1_1012+2insCG
ENST00000461903.1:n.1254_1255insCG
ENST00000479320.5:n.1253+1_1253+2insCG
ENST00000495183.5:n.1255+1_1255+2insCG
ENST00000496081.5:n.830_831insCG
NM_002116.7:c.1012+1_1012+2insCG	NP_002107.3:n.1012+1_1012+2insCG
NM_002116.8:c.1012+1_1012+2insCG MANE Select	NP_002107.3:n.1012+1_1012+2insCG