Canonical Allele Identifier: CA2843412374

Gene: WARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119033116del , CM000663.2:g.119033116del	GRCh38
NC_000001.10:g.119575739del , CM000663.1:g.119575739del	GRCh37
NC_000001.9:g.119377262del	NCBI36
NG_050658.1:g.112673del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235521.5:c.878del MANE Select	ENSP00000235521.4:p.Arg293ProfsTer5
ENST00000235521.4:c.878del	ENSP00000235521.4:p.Arg293ProfsTer5
ENST00000369426.9:c.*244del	ENSP00000358434.5:n.*244del
NM_015836.3:c.878del	NP_056651.1:p.Arg293ProfsTer5
NM_201263.2:c.*244del	NP_957715.1:n.*244del
XM_005270350.2:c.824del	XP_005270407.1:p.Arg275ProfsTer5
XM_006710283.1:c.596del	XP_006710346.1:p.Arg199ProfsTer5
XM_011540493.1:c.809del	XP_011538795.1:p.Arg270ProfsTer5
XM_011540494.1:c.809del	XP_011538796.1:p.Arg270ProfsTer5
XM_011540495.1:c.620del	XP_011538797.1:p.Arg207ProfsTer5
XM_005270350.3:c.824del	XP_005270407.1:p.Arg275ProfsTer5
XM_011540494.2:c.809del	XP_011538796.1:p.Arg270ProfsTer5
XM_011540495.2:c.620del	XP_011538797.1:p.Arg207ProfsTer5
XM_017000038.1:c.821del	XP_016855527.1:p.Arg274ProfsTer5
XM_017000039.1:c.809del	XP_016855528.1:p.Arg270ProfsTer5
XM_017000040.1:c.707del	XP_016855529.1:p.Arg236ProfsTer5
XM_017000041.2:c.539del	XP_016855530.1:p.Arg180ProfsTer5
XM_017000042.1:c.*213del	XP_016855531.1:n.*213del
XM_024449826.1:c.809del	XP_024305594.1:p.Arg270ProfsTer5
XM_024449860.1:c.596del	XP_024305628.1:p.Arg199ProfsTer5
XM_024449871.1:c.596del	XP_024305639.1:p.Arg199ProfsTer5
NM_001378226.1:c.809del	NP_001365155.1:p.Arg270ProfsTer5
NM_001378227.1:c.809del	NP_001365156.1:p.Arg270ProfsTer5
NM_001378228.1:c.707del	NP_001365157.1:p.Arg236ProfsTer5
NM_001378229.1:c.620del	NP_001365158.1:p.Arg207ProfsTer5
NM_001378230.1:c.596del	NP_001365159.1:p.Arg199ProfsTer5
NM_001378231.1:c.*213del	NP_001365160.1:n.*213del
NM_015836.4:c.878del MANE Select	NP_056651.1:p.Arg293ProfsTer5