Canonical Allele Identifier: CA2840060542
Gene: HLA-A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29943445_29943456del , CM000668.2:g.29943445_29943456del GRCh38
NC_000006.11:g.29911222_29911233del , CM000668.1:g.29911222_29911233del GRCh37
NC_000006.10:g.30019201_30019212del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.521_532del ENSP00000492789.2:p.Ala174_Ala177del
ENST00000706892.1:n.797_808del
ENST00000706893.1:c.521_532del ENSP00000516609.1:p.Ala174_Ala177del
ENST00000706894.1:c.521_532del ENSP00000516610.1:p.Ala174_Ala177del
ENST00000706895.1:n.797_808del
ENST00000706896.1:n.797_808del
ENST00000706897.1:n.797_808del
ENST00000706898.1:c.521_532del ENSP00000516611.1:p.Ala174_Ala177del
ENST00000706899.1:n.797_808del
ENST00000706900.1:c.437_448del ENSP00000516617.1:p.Ala146_Ala149del
ENST00000706901.1:c.521_532del ENSP00000516612.1:p.Ala174_Ala177del
ENST00000706902.1:c.521_532del ENSP00000516613.1:p.Ala174_Ala177del
ENST00000706903.1:c.521_532del ENSP00000516614.1:p.Ala174_Ala177del
ENST00000706904.1:c.521_532del ENSP00000516615.1:p.Ala174_Ala177del
ENST00000706905.1:c.521_532del ENSP00000516616.1:p.Ala174_Ala177del
ENST00000376809.10:c.521_532del MANE Select ENSP00000366005.5:p.Ala174_Ala177del
ENST00000638375.1:c.521_532del ENSP00000492789.1:p.Ala174_Ala177del
ENST00000376802.2:c.521_532del ENSP00000365998.2:p.Ala174_Ala177del
ENST00000376806.9:c.521_532del ENSP00000366002.5:p.Ala174_Ala177del
ENST00000376809.9:c.521_532del ENSP00000366005.5:p.Ala174_Ala177del
ENST00000396634.5:c.521_532del ENSP00000379873.1:p.Ala174_Ala177del
ENST00000461903.1:n.762_773del
ENST00000479320.5:n.762_773del
ENST00000495183.5:n.764_775del
ENST00000496081.5:n.338_349del
NM_002116.7:c.521_532del NP_002107.3:p.Ala174_Ala177del
NM_002116.8:c.521_532del MANE Select NP_002107.3:p.Ala174_Ala177del