Canonical Allele Identifier: CA2677796570

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29945256-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945257del , CM000668.2:g.29945257del	GRCh38
NC_000006.11:g.29913034del , CM000668.1:g.29913034del	GRCh37
NC_000006.10:g.30021013del	NCBI36
NG_029217.2:g.7793del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.952del	ENSP00000492789.2:p.Asp318MetfsTer29
ENST00000706892.1:n.2609del
ENST00000706893.1:c.*53del	ENSP00000516609.1:n.*53del
ENST00000706894.1:c.1069del	ENSP00000516610.1:p.Asp357MetfsTer15
ENST00000706895.1:n.1889del
ENST00000706896.1:n.2365del
ENST00000706897.1:n.1787del
ENST00000706898.1:c.1087del	ENSP00000516611.1:p.Asp363MetfsTer29
ENST00000706899.1:n.1923del
ENST00000706900.1:c.985del	ENSP00000516617.1:p.Asp329MetfsTer29
ENST00000706901.1:c.1069del	ENSP00000516612.1:p.Asp357MetfsTer29
ENST00000706902.1:c.1069del	ENSP00000516613.1:p.Asp357MetfsTer16
ENST00000706903.1:c.1069del	ENSP00000516614.1:p.Asp357MetfsTer29
ENST00000706904.1:c.1069del	ENSP00000516615.1:p.Asp357MetfsTer16
ENST00000706905.1:c.1069del	ENSP00000516616.1:p.Asp357MetfsTer29
ENST00000376809.10:c.1069del MANE Select	ENSP00000366005.5:p.Asp357MetfsTer29
ENST00000638375.1:c.952del	ENSP00000492789.1:p.Asp318MetfsTer?
ENST00000376802.2:c.896-194del	ENSP00000365998.2:n.896-194del
ENST00000376806.9:c.1087del	ENSP00000366002.5:p.Asp363MetfsTer29
ENST00000376809.9:c.1069del	ENSP00000366005.5:p.Asp357MetfsTer29
ENST00000396634.5:c.1069del	ENSP00000379873.1:p.Asp357MetfsTer29
ENST00000461903.1:n.1328del
ENST00000479320.5:n.1310del
ENST00000495183.5:n.1308del
ENST00000496081.5:n.1328del
NM_002116.7:c.1069del	NP_002107.3:p.Asp357MetfsTer29
NM_002116.8:c.1069del MANE Select	NP_002107.3:p.Asp357MetfsTer29