Canonical Allele Identifier: CA420192864

Gene: WARS2

Linked Data

• MyVariant Identifiers: chr1:g.119575900T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119033277T>G , CM000663.2:g.119033277T>G	GRCh38
NC_000001.10:g.119575900T>G , CM000663.1:g.119575900T>G	GRCh37
NC_000001.9:g.119377423T>G	NCBI36
NG_050658.1:g.112512A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235521.5:c.717A>C MANE Select	ENSP00000235521.4:p.Arg239=
ENST00000235521.4:c.717A>C	ENSP00000235521.4:p.Arg239=
ENST00000369426.9:c.*83A>C	ENSP00000358434.5:n.*83A>C
NM_015836.3:c.717A>C	NP_056651.1:p.Arg239=
NM_201263.2:c.*83A>C	NP_957715.1:n.*83A>C
XM_005270350.2:c.663A>C	XP_005270407.1:p.Arg221=
XM_006710283.1:c.435A>C	XP_006710346.1:p.Arg145=
XM_011540493.1:c.648A>C	XP_011538795.1:p.Arg216=
XM_011540494.1:c.648A>C	XP_011538796.1:p.Arg216=
XM_011540495.1:c.459A>C	XP_011538797.1:p.Arg153=
XM_005270350.3:c.663A>C	XP_005270407.1:p.Arg221=
XM_011540494.2:c.648A>C	XP_011538796.1:p.Arg216=
XM_011540495.2:c.459A>C	XP_011538797.1:p.Arg153=
XM_017000038.1:c.660A>C	XP_016855527.1:p.Arg220=
XM_017000039.1:c.648A>C	XP_016855528.1:p.Arg216=
XM_017000040.1:c.546A>C	XP_016855529.1:p.Arg182=
XM_017000041.2:c.378A>C	XP_016855530.1:p.Arg126=
XM_017000042.1:c.*52A>C	XP_016855531.1:n.*52A>C
XM_024449826.1:c.648A>C	XP_024305594.1:p.Arg216=
XM_024449860.1:c.435A>C	XP_024305628.1:p.Arg145=
XM_024449871.1:c.435A>C	XP_024305639.1:p.Arg145=
NM_001378226.1:c.648A>C	NP_001365155.1:p.Arg216=
NM_001378227.1:c.648A>C	NP_001365156.1:p.Arg216=
NM_001378228.1:c.546A>C	NP_001365157.1:p.Arg182=
NM_001378229.1:c.459A>C	NP_001365158.1:p.Arg153=
NM_001378230.1:c.435A>C	NP_001365159.1:p.Arg145=
NM_001378231.1:c.*52A>C	NP_001365160.1:n.*52A>C
NM_015836.4:c.717A>C MANE Select	NP_056651.1:p.Arg239=