Canonical Allele Identifier: CA1192128223

Gene: WARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119033278C= , CM000663.2:g.119033278C=	GRCh38
NC_000001.10:g.119575901C= , CM000663.1:g.119575901C=	GRCh37
NC_000001.9:g.119377424C=	NCBI36
NG_050658.1:g.112511G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235521.5:c.716G= MANE Select	ENSP00000235521.4:p.Arg239=
ENST00000235521.4:c.716G=	ENSP00000235521.4:p.Arg239=
ENST00000369426.9:c.*82G=	ENSP00000358434.5:n.*82G=
NM_015836.3:c.716G=	NP_056651.1:p.Arg239=
NM_201263.2:c.*82G=	NP_957715.1:n.*82G=
XM_005270350.2:c.662G=	XP_005270407.1:p.Arg221=
XM_006710283.1:c.434G=	XP_006710346.1:p.Arg145=
XM_011540493.1:c.647G=	XP_011538795.1:p.Arg216=
XM_011540494.1:c.647G=	XP_011538796.1:p.Arg216=
XM_011540495.1:c.458G=	XP_011538797.1:p.Arg153=
XM_005270350.3:c.662G=	XP_005270407.1:p.Arg221=
XM_011540494.2:c.647G=	XP_011538796.1:p.Arg216=
XM_011540495.2:c.458G=	XP_011538797.1:p.Arg153=
XM_017000038.1:c.659G=	XP_016855527.1:p.Arg220=
XM_017000039.1:c.647G=	XP_016855528.1:p.Arg216=
XM_017000040.1:c.545G=	XP_016855529.1:p.Arg182=
XM_017000041.2:c.377G=	XP_016855530.1:p.Arg126=
XM_017000042.1:c.*51G=	XP_016855531.1:n.*51G=
XM_024449826.1:c.647G=	XP_024305594.1:p.Arg216=
XM_024449860.1:c.434G=	XP_024305628.1:p.Arg145=
XM_024449871.1:c.434G=	XP_024305639.1:p.Arg145=
NM_001378226.1:c.647G=	NP_001365155.1:p.Arg216=
NM_001378227.1:c.647G=	NP_001365156.1:p.Arg216=
NM_001378228.1:c.545G=	NP_001365157.1:p.Arg182=
NM_001378229.1:c.458G=	NP_001365158.1:p.Arg153=
NM_001378230.1:c.434G=	NP_001365159.1:p.Arg145=
NM_001378231.1:c.*51G=	NP_001365160.1:n.*51G=
NM_015836.4:c.716G= MANE Select	NP_056651.1:p.Arg239=