Canonical Allele Identifier: CA2838620751
Gene: WARS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.119033166del , CM000663.2:g.119033166del GRCh38
NC_000001.10:g.119575789del , CM000663.1:g.119575789del GRCh37
NC_000001.9:g.119377312del NCBI36
NG_050658.1:g.112624del

Transcript Alleles

HGVS Amino-acid Change
ENST00000235521.5:c.829del MANE Select ENSP00000235521.4:p.Ala277ArgfsTer6
ENST00000235521.4:c.829del ENSP00000235521.4:p.Ala277ArgfsTer6
ENST00000369426.9:c.*195del ENSP00000358434.5:n.*195del
NM_015836.3:c.829del NP_056651.1:p.Ala277ArgfsTer6
NM_201263.2:c.*195del NP_957715.1:n.*195del
XM_005270350.2:c.775del XP_005270407.1:p.Ala259ArgfsTer6
XM_006710283.1:c.547del XP_006710346.1:p.Ala183ArgfsTer6
XM_011540493.1:c.760del XP_011538795.1:p.Ala254ArgfsTer6
XM_011540494.1:c.760del XP_011538796.1:p.Ala254ArgfsTer6
XM_011540495.1:c.571del XP_011538797.1:p.Ala191ArgfsTer6
XM_005270350.3:c.775del XP_005270407.1:p.Ala259ArgfsTer6
XM_011540494.2:c.760del XP_011538796.1:p.Ala254ArgfsTer6
XM_011540495.2:c.571del XP_011538797.1:p.Ala191ArgfsTer6
XM_017000038.1:c.772del XP_016855527.1:p.Ala258ArgfsTer6
XM_017000039.1:c.760del XP_016855528.1:p.Ala254ArgfsTer6
XM_017000040.1:c.658del XP_016855529.1:p.Ala220ArgfsTer6
XM_017000041.2:c.490del XP_016855530.1:p.Ala164ArgfsTer6
XM_017000042.1:c.*164del XP_016855531.1:n.*164del
XM_024449826.1:c.760del XP_024305594.1:p.Ala254ArgfsTer6
XM_024449860.1:c.547del XP_024305628.1:p.Ala183ArgfsTer6
XM_024449871.1:c.547del XP_024305639.1:p.Ala183ArgfsTer6
NM_001378226.1:c.760del NP_001365155.1:p.Ala254ArgfsTer6
NM_001378227.1:c.760del NP_001365156.1:p.Ala254ArgfsTer6
NM_001378228.1:c.658del NP_001365157.1:p.Ala220ArgfsTer6
NM_001378229.1:c.571del NP_001365158.1:p.Ala191ArgfsTer6
NM_001378230.1:c.547del NP_001365159.1:p.Ala183ArgfsTer6
NM_001378231.1:c.*164del NP_001365160.1:n.*164del
NM_015836.4:c.829del MANE Select NP_056651.1:p.Ala277ArgfsTer6