Canonical Allele Identifier: CA2677794655

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29944525-CAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29944526_29944527del , CM000668.2:g.29944526_29944527del	GRCh38
NC_000006.11:g.29912303_29912304del , CM000668.1:g.29912303_29912304del	GRCh37
NC_000006.10:g.30020282_30020283del	NCBI36
NG_029217.2:g.7062_7063del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.895+129_895+130del	ENSP00000492789.2:n.895+129_895+130del
ENST00000706892.1:n.1878_1879del
ENST00000706893.1:c.956_957del	ENSP00000516609.1:p.His319ProfsTer14
ENST00000706894.1:c.922_923del	ENSP00000516610.1:p.Ile308ArgfsTer?
ENST00000706895.1:n.1300_1301del
ENST00000706896.1:n.1776_1777del
ENST00000706897.1:n.1198_1199del
ENST00000706898.1:c.922_923del	ENSP00000516611.1:p.Ile308ArgfsTer?
ENST00000706899.1:n.1776_1777del
ENST00000706900.1:c.838_839del	ENSP00000516617.1:p.Ile280ArgfsTer?
ENST00000706901.1:c.922_923del	ENSP00000516612.1:p.Ile308ArgfsTer?
ENST00000706902.1:c.922_923del	ENSP00000516613.1:p.Ile308ArgfsTer?
ENST00000706903.1:c.922_923del	ENSP00000516614.1:p.Ile308ArgfsTer?
ENST00000706904.1:c.922_923del	ENSP00000516615.1:p.Ile308ArgfsTer?
ENST00000706905.1:c.922_923del	ENSP00000516616.1:p.Ile308ArgfsTer?
ENST00000376809.10:c.922_923del MANE Select	ENSP00000366005.5:p.Ile308ArgfsTer?
ENST00000638375.1:c.895+129_895+130del	ENSP00000492789.1:n.895+129_895+130del
ENST00000376802.2:c.895+129_895+130del	ENSP00000365998.2:n.895+129_895+130del
ENST00000376806.9:c.922_923del	ENSP00000366002.5:p.Ile308ArgfsTer?
ENST00000376809.9:c.922_923del	ENSP00000366005.5:p.Ile308ArgfsTer?
ENST00000396634.5:c.922_923del	ENSP00000379873.1:p.Ile308ArgfsTer?
ENST00000461903.1:n.1163_1164del
ENST00000479320.5:n.1163_1164del
ENST00000495183.5:n.1165_1166del
ENST00000496081.5:n.739_740del
NM_002116.7:c.922_923del	NP_002107.3:p.Ile308ArgfsTer?
NM_002116.8:c.922_923del MANE Select	NP_002107.3:p.Ile308ArgfsTer?