Canonical Allele Identifier: CA420192882

Gene: WARS2

Linked Data

• MyVariant Identifiers: chr1:g.119575912C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119033289C>G , CM000663.2:g.119033289C>G	GRCh38
NC_000001.10:g.119575912C>G , CM000663.1:g.119575912C>G	GRCh37
NC_000001.9:g.119377435C>G	NCBI36
NG_050658.1:g.112500G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235521.5:c.705G>C MANE Select	ENSP00000235521.4:p.Leu235=
ENST00000235521.4:c.705G>C	ENSP00000235521.4:p.Leu235=
ENST00000369426.9:c.*71G>C	ENSP00000358434.5:n.*71G>C
NM_015836.3:c.705G>C	NP_056651.1:p.Leu235=
NM_201263.2:c.*71G>C	NP_957715.1:n.*71G>C
XM_005270350.2:c.651G>C	XP_005270407.1:p.Leu217=
XM_006710283.1:c.423G>C	XP_006710346.1:p.Leu141=
XM_011540493.1:c.636G>C	XP_011538795.1:p.Leu212=
XM_011540494.1:c.636G>C	XP_011538796.1:p.Leu212=
XM_011540495.1:c.447G>C	XP_011538797.1:p.Leu149=
XM_005270350.3:c.651G>C	XP_005270407.1:p.Leu217=
XM_011540494.2:c.636G>C	XP_011538796.1:p.Leu212=
XM_011540495.2:c.447G>C	XP_011538797.1:p.Leu149=
XM_017000038.1:c.648G>C	XP_016855527.1:p.Leu216=
XM_017000039.1:c.636G>C	XP_016855528.1:p.Leu212=
XM_017000040.1:c.534G>C	XP_016855529.1:p.Leu178=
XM_017000041.2:c.366G>C	XP_016855530.1:p.Leu122=
XM_017000042.1:c.*40G>C	XP_016855531.1:n.*40G>C
XM_024449826.1:c.636G>C	XP_024305594.1:p.Leu212=
XM_024449860.1:c.423G>C	XP_024305628.1:p.Leu141=
XM_024449871.1:c.423G>C	XP_024305639.1:p.Leu141=
NM_001378226.1:c.636G>C	NP_001365155.1:p.Leu212=
NM_001378227.1:c.636G>C	NP_001365156.1:p.Leu212=
NM_001378228.1:c.534G>C	NP_001365157.1:p.Leu178=
NM_001378229.1:c.447G>C	NP_001365158.1:p.Leu149=
NM_001378230.1:c.423G>C	NP_001365159.1:p.Leu141=
NM_001378231.1:c.*40G>C	NP_001365160.1:n.*40G>C
NM_015836.4:c.705G>C MANE Select	NP_056651.1:p.Leu235=