Canonical Allele Identifier: CA341436621

Gene: WARS2

Linked Data

• COSMIC: COSM4021236
• MyVariant Identifiers: chr1:g.119575832A>G (hg19) ; chr1:g.119033209A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119033209A>G , CM000663.2:g.119033209A>G	GRCh38
NC_000001.10:g.119575832A>G , CM000663.1:g.119575832A>G	GRCh37
NC_000001.9:g.119377355A>G	NCBI36
NG_050658.1:g.112580T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235521.5:c.785T>C MANE Select	ENSP00000235521.4:p.Val262Ala
ENST00000235521.4:c.785T>C	ENSP00000235521.4:p.Val262Ala
ENST00000369426.9:c.*151T>C	ENSP00000358434.5:n.*151T>C
NM_015836.3:c.785T>C	NP_056651.1:p.Val262Ala
NM_201263.2:c.*151T>C	NP_957715.1:n.*151T>C
XM_005270350.2:c.731T>C	XP_005270407.1:p.Val244Ala
XM_006710283.1:c.503T>C	XP_006710346.1:p.Val168Ala
XM_011540493.1:c.716T>C	XP_011538795.1:p.Val239Ala
XM_011540494.1:c.716T>C	XP_011538796.1:p.Val239Ala
XM_011540495.1:c.527T>C	XP_011538797.1:p.Val176Ala
XM_005270350.3:c.731T>C	XP_005270407.1:p.Val244Ala
XM_011540494.2:c.716T>C	XP_011538796.1:p.Val239Ala
XM_011540495.2:c.527T>C	XP_011538797.1:p.Val176Ala
XM_017000038.1:c.728T>C	XP_016855527.1:p.Val243Ala
XM_017000039.1:c.716T>C	XP_016855528.1:p.Val239Ala
XM_017000040.1:c.614T>C	XP_016855529.1:p.Val205Ala
XM_017000041.2:c.446T>C	XP_016855530.1:p.Val149Ala
XM_017000042.1:c.*120T>C	XP_016855531.1:n.*120T>C
XM_024449826.1:c.716T>C	XP_024305594.1:p.Val239Ala
XM_024449860.1:c.503T>C	XP_024305628.1:p.Val168Ala
XM_024449871.1:c.503T>C	XP_024305639.1:p.Val168Ala
NM_001378226.1:c.716T>C	NP_001365155.1:p.Val239Ala
NM_001378227.1:c.716T>C	NP_001365156.1:p.Val239Ala
NM_001378228.1:c.614T>C	NP_001365157.1:p.Val205Ala
NM_001378229.1:c.527T>C	NP_001365158.1:p.Val176Ala
NM_001378230.1:c.503T>C	NP_001365159.1:p.Val168Ala
NM_001378231.1:c.*120T>C	NP_001365160.1:n.*120T>C
NM_015836.4:c.785T>C MANE Select	NP_056651.1:p.Val262Ala