Canonical Allele Identifier: CA2677793887

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29942781-T-TCAC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29942782_29942784dup , CM000668.2:g.29942782_29942784dup	GRCh38
NC_000006.11:g.29910559_29910561dup , CM000668.1:g.29910559_29910561dup	GRCh37
NC_000006.10:g.30018538_30018540dup	NCBI36
NG_029217.2:g.5317_5319dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000638375.2:c.99_101dup	ENSP00000492789.2:p.Thr34_Ser35insThr
ENST00000706892.1:n.375_377dup
ENST00000706893.1:c.99_101dup	ENSP00000516609.1:p.Thr34_Ser35insThr
ENST00000706894.1:c.99_101dup	ENSP00000516610.1:p.Thr34_Ser35insThr
ENST00000706895.1:n.375_377dup
ENST00000706896.1:n.375_377dup
ENST00000706897.1:n.375_377dup
ENST00000706898.1:c.99_101dup	ENSP00000516611.1:p.Thr34_Ser35insThr
ENST00000706899.1:n.375_377dup
ENST00000706900.1:c.15_17dup	ENSP00000516617.1:p.Thr6_Ser7insThr
ENST00000706901.1:c.99_101dup	ENSP00000516612.1:p.Thr34_Ser35insThr
ENST00000706902.1:c.99_101dup	ENSP00000516613.1:p.Thr34_Ser35insThr
ENST00000706903.1:c.99_101dup	ENSP00000516614.1:p.Thr34_Ser35insThr
ENST00000706904.1:c.99_101dup	ENSP00000516615.1:p.Thr34_Ser35insThr
ENST00000706905.1:c.99_101dup	ENSP00000516616.1:p.Thr34_Ser35insThr
ENST00000376809.10:c.99_101dup MANE Select	ENSP00000366005.5:p.Thr34_Ser35insThr
ENST00000638375.1:c.99_101dup	ENSP00000492789.1:p.Thr34_Ser35insThr
ENST00000376802.2:c.99_101dup	ENSP00000365998.2:p.Thr34_Ser35insThr
ENST00000376806.9:c.99_101dup	ENSP00000366002.5:p.Thr34_Ser35insThr
ENST00000376809.9:c.99_101dup	ENSP00000366005.5:p.Thr34_Ser35insThr
ENST00000396634.5:c.99_101dup	ENSP00000379873.1:p.Thr34_Ser35insThr
ENST00000429656.1:n.284_286dup
ENST00000461903.1:n.99_101dup
ENST00000479320.5:n.99_101dup
ENST00000495183.5:n.101_103dup
ENST00000496081.5:n.105_107dup
NM_002116.7:c.99_101dup	NP_002107.3:p.Thr34_Ser35insThr
NM_002116.8:c.99_101dup MANE Select	NP_002107.3:p.Thr34_Ser35insThr