Canonical Allele Identifier: CA2770466755
Gene: HLA-A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29942593_29942594insTGGG , CM000668.2:g.29942593_29942594insTGGG GRCh38
NC_000006.11:g.29910370_29910371insTGGG , CM000668.1:g.29910370_29910371insTGGG GRCh37
NC_000006.10:g.30018349_30018350insTGGG NCBI36
NG_029217.2:g.5128_5129insTGGG

Transcript Alleles

HGVS Amino-acid change
ENST00000638375.2:c.40_41insTGGG ENSP00000492789.2:p.Ser14LeufsTer?
ENST00000706892.1:n.316_317insTGGG
ENST00000706893.1:c.40_41insTGGG ENSP00000516609.1:p.Ser14LeufsTer?
ENST00000706894.1:c.40_41insTGGG ENSP00000516610.1:p.Ser14LeufsTer?
ENST00000706895.1:n.316_317insTGGG
ENST00000706896.1:n.316_317insTGGG
ENST00000706897.1:n.316_317insTGGG
ENST00000706898.1:c.40_41insTGGG ENSP00000516611.1:p.Ser14LeufsTer?
ENST00000706899.1:n.316_317insTGGG
ENST00000706901.1:c.40_41insTGGG ENSP00000516612.1:p.Ser14LeufsTer?
ENST00000706902.1:c.40_41insTGGG ENSP00000516613.1:p.Ser14LeufsTer?
ENST00000706903.1:c.40_41insTGGG ENSP00000516614.1:p.Ser14LeufsTer?
ENST00000706904.1:c.40_41insTGGG ENSP00000516615.1:p.Ser14LeufsTer?
ENST00000706905.1:c.40_41insTGGG ENSP00000516616.1:p.Ser14LeufsTer?
ENST00000376809.10:c.40_41insTGGG MANE Select ENSP00000366005.5:p.Ser14LeufsTer?
ENST00000638375.1:c.40_41insTGGG ENSP00000492789.1:p.Ser14LeufsTer?
ENST00000376802.2:c.40_41insTGGG ENSP00000365998.2:p.Ser14LeufsTer?
ENST00000376806.9:c.40_41insTGGG ENSP00000366002.5:p.Ser14LeufsTer?
ENST00000376809.9:c.40_41insTGGG ENSP00000366005.5:p.Ser14LeufsTer?
ENST00000396634.5:c.40_41insTGGG ENSP00000379873.1:p.Ser14LeufsTer?
ENST00000429656.1:n.474_475insCCCA
ENST00000461903.1:n.40_41insTGGG
ENST00000479320.5:n.40_41insTGGG
ENST00000495183.5:n.42_43insTGGG
ENST00000496081.5:n.46_47insTGGG
NM_002116.7:c.40_41insTGGG NP_002107.3:p.Ser14LeufsTer?
NM_002116.8:c.40_41insTGGG MANE Select NP_002107.3:p.Ser14LeufsTer?