Canonical Allele Identifier: CA2677794501

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29944400-AAGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29944404_29944406del , CM000668.2:g.29944404_29944406del	GRCh38
NC_000006.11:g.29912181_29912183del , CM000668.1:g.29912181_29912183del	GRCh37
NC_000006.10:g.30020160_30020162del	NCBI36
NG_029217.2:g.6940_6942del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.895+7_895+9del	ENSP00000492789.2:n.895+7_895+9del
ENST00000706892.1:n.1756_1758del
ENST00000706893.1:c.895+7_895+9del	ENSP00000516609.1:n.895+7_895+9del
ENST00000706894.1:c.895+7_895+9del	ENSP00000516610.1:n.895+7_895+9del
ENST00000706895.1:n.1178_1180del
ENST00000706896.1:n.1749+7_1749+9del
ENST00000706897.1:n.1171+7_1171+9del
ENST00000706898.1:c.895+7_895+9del	ENSP00000516611.1:n.895+7_895+9del
ENST00000706899.1:n.1749+7_1749+9del
ENST00000706900.1:c.811+7_811+9del	ENSP00000516617.1:n.811+7_811+9del
ENST00000706901.1:c.895+7_895+9del	ENSP00000516612.1:n.895+7_895+9del
ENST00000706902.1:c.895+7_895+9del	ENSP00000516613.1:n.895+7_895+9del
ENST00000706903.1:c.895+7_895+9del	ENSP00000516614.1:n.895+7_895+9del
ENST00000706904.1:c.895+7_895+9del	ENSP00000516615.1:n.895+7_895+9del
ENST00000706905.1:c.895+7_895+9del	ENSP00000516616.1:n.895+7_895+9del
ENST00000376809.10:c.895+7_895+9del MANE Select	ENSP00000366005.5:n.895+7_895+9del
ENST00000638375.1:c.895+7_895+9del	ENSP00000492789.1:n.895+7_895+9del
ENST00000376802.2:c.895+7_895+9del	ENSP00000365998.2:n.895+7_895+9del
ENST00000376806.9:c.895+7_895+9del	ENSP00000366002.5:n.895+7_895+9del
ENST00000376809.9:c.895+7_895+9del	ENSP00000366005.5:n.895+7_895+9del
ENST00000396634.5:c.895+7_895+9del	ENSP00000379873.1:n.895+7_895+9del
ENST00000461903.1:n.1136+7_1136+9del
ENST00000479320.5:n.1136+7_1136+9del
ENST00000495183.5:n.1138+7_1138+9del
ENST00000496081.5:n.712+7_712+9del
NM_002116.7:c.895+7_895+9del	NP_002107.3:n.895+7_895+9del
NM_002116.8:c.895+7_895+9del MANE Select	NP_002107.3:n.895+7_895+9del