Canonical Allele Identifier: CA2838620754
Gene: WARS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.119033131dup , CM000663.2:g.119033131dup GRCh38
NC_000001.10:g.119575754dup , CM000663.1:g.119575754dup GRCh37
NC_000001.9:g.119377277dup NCBI36
NG_050658.1:g.112658dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000235521.5:c.863dup MANE Select ENSP00000235521.4:p.Glu289GlyfsTer24
ENST00000235521.4:c.863dup ENSP00000235521.4:p.Glu289GlyfsTer24
ENST00000369426.9:c.*229dup ENSP00000358434.5:n.*229dup
NM_015836.3:c.863dup NP_056651.1:p.Glu289GlyfsTer24
NM_201263.2:c.*229dup NP_957715.1:n.*229dup
XM_005270350.2:c.809dup XP_005270407.1:p.Glu271GlyfsTer24
XM_006710283.1:c.581dup XP_006710346.1:p.Glu195GlyfsTer24
XM_011540493.1:c.794dup XP_011538795.1:p.Glu266GlyfsTer24
XM_011540494.1:c.794dup XP_011538796.1:p.Glu266GlyfsTer24
XM_011540495.1:c.605dup XP_011538797.1:p.Glu203GlyfsTer24
XM_005270350.3:c.809dup XP_005270407.1:p.Glu271GlyfsTer24
XM_011540494.2:c.794dup XP_011538796.1:p.Glu266GlyfsTer24
XM_011540495.2:c.605dup XP_011538797.1:p.Glu203GlyfsTer24
XM_017000038.1:c.806dup XP_016855527.1:p.Glu270GlyfsTer24
XM_017000039.1:c.794dup XP_016855528.1:p.Glu266GlyfsTer24
XM_017000040.1:c.692dup XP_016855529.1:p.Glu232GlyfsTer24
XM_017000041.2:c.524dup XP_016855530.1:p.Glu176GlyfsTer24
XM_017000042.1:c.*198dup XP_016855531.1:n.*198dup
XM_024449826.1:c.794dup XP_024305594.1:p.Glu266GlyfsTer24
XM_024449860.1:c.581dup XP_024305628.1:p.Glu195GlyfsTer24
XM_024449871.1:c.581dup XP_024305639.1:p.Glu195GlyfsTer24
NM_001378226.1:c.794dup NP_001365155.1:p.Glu266GlyfsTer24
NM_001378227.1:c.794dup NP_001365156.1:p.Glu266GlyfsTer24
NM_001378228.1:c.692dup NP_001365157.1:p.Glu232GlyfsTer24
NM_001378229.1:c.605dup NP_001365158.1:p.Glu203GlyfsTer24
NM_001378230.1:c.581dup NP_001365159.1:p.Glu195GlyfsTer24
NM_001378231.1:c.*198dup NP_001365160.1:n.*198dup
NM_015836.4:c.863dup MANE Select NP_056651.1:p.Glu289GlyfsTer24