Canonical Allele Identifier: CA1618519556

Gene: HLA-A

Linked Data

• dbSNP Id: rs1771449343
• gnomAD v4: 6-29944557-TTGGAGCTGTGATCAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29944568_29944582del , CM000668.2:g.29944568_29944582del	GRCh38
NC_000006.11:g.29912345_29912359del , CM000668.1:g.29912345_29912359del	GRCh37
NC_000006.10:g.30020324_30020338del	NCBI36
NG_029217.2:g.7104_7118del

Transcript Alleles

HGVS	Amino-acid change
ENST00000638375.2:c.895+171_895+185del	ENSP00000492789.2:n.895+171_895+185del
ENST00000706892.1:n.1920_1934del
ENST00000706893.1:c.998_1012del	ENSP00000516609.1:p.Asp333_Cys337del
ENST00000706894.1:c.964_978del	ENSP00000516610.1:p.Ile322_Val326del
ENST00000706895.1:n.1342_1356del
ENST00000706896.1:n.1818_1832del
ENST00000706897.1:n.1240_1254del
ENST00000706898.1:c.964_978del	ENSP00000516611.1:p.Ile322_Val326del
ENST00000706899.1:n.1818_1832del
ENST00000706900.1:c.880_894del	ENSP00000516617.1:p.Ile294_Val298del
ENST00000706901.1:c.964_978del	ENSP00000516612.1:p.Ile322_Val326del
ENST00000706902.1:c.964_978del	ENSP00000516613.1:p.Ile322_Val326del
ENST00000706903.1:c.964_978del	ENSP00000516614.1:p.Ile322_Val326del
ENST00000706904.1:c.964_978del	ENSP00000516615.1:p.Ile322_Val326del
ENST00000706905.1:c.964_978del	ENSP00000516616.1:p.Ile322_Val326del
ENST00000376809.10:c.964_978del MANE Select	ENSP00000366005.5:p.Ile322_Val326del
ENST00000638375.1:c.895+171_895+185del	ENSP00000492789.1:n.895+171_895+185del
ENST00000376802.2:c.895+171_895+185del	ENSP00000365998.2:n.895+171_895+185del
ENST00000376806.9:c.964_978del	ENSP00000366002.5:p.Ile322_Val326del
ENST00000376809.9:c.964_978del	ENSP00000366005.5:p.Ile322_Val326del
ENST00000396634.5:c.964_978del	ENSP00000379873.1:p.Ile322_Val326del
ENST00000461903.1:n.1205_1219del
ENST00000479320.5:n.1205_1219del
ENST00000495183.5:n.1207_1221del
ENST00000496081.5:n.781_795del
NM_002116.7:c.964_978del	NP_002107.3:p.Ile322_Val326del
NM_002116.8:c.964_978del MANE Select	NP_002107.3:p.Ile322_Val326del