Canonical Allele Identifier: CA341436697

Gene: WARS2

Linked Data

• dbSNP Id: rs1557929151
• MyVariant Identifiers: chr1:g.119575866A>T (hg19) ; chr1:g.119033243A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119033243A>T , CM000663.2:g.119033243A>T	GRCh38
NC_000001.10:g.119575866A>T , CM000663.1:g.119575866A>T	GRCh37
NC_000001.9:g.119377389A>T	NCBI36
NG_050658.1:g.112546T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235521.5:c.751T>A MANE Select	ENSP00000235521.4:p.Phe251Ile
ENST00000235521.4:c.751T>A	ENSP00000235521.4:p.Phe251Ile
ENST00000369426.9:c.*117T>A	ENSP00000358434.5:n.*117T>A
NM_015836.3:c.751T>A	NP_056651.1:p.Phe251Ile
NM_201263.2:c.*117T>A	NP_957715.1:n.*117T>A
XM_005270350.2:c.697T>A	XP_005270407.1:p.Phe233Ile
XM_006710283.1:c.469T>A	XP_006710346.1:p.Phe157Ile
XM_011540493.1:c.682T>A	XP_011538795.1:p.Phe228Ile
XM_011540494.1:c.682T>A	XP_011538796.1:p.Phe228Ile
XM_011540495.1:c.493T>A	XP_011538797.1:p.Phe165Ile
XM_005270350.3:c.697T>A	XP_005270407.1:p.Phe233Ile
XM_011540494.2:c.682T>A	XP_011538796.1:p.Phe228Ile
XM_011540495.2:c.493T>A	XP_011538797.1:p.Phe165Ile
XM_017000038.1:c.694T>A	XP_016855527.1:p.Phe232Ile
XM_017000039.1:c.682T>A	XP_016855528.1:p.Phe228Ile
XM_017000040.1:c.580T>A	XP_016855529.1:p.Phe194Ile
XM_017000041.2:c.412T>A	XP_016855530.1:p.Phe138Ile
XM_017000042.1:c.*86T>A	XP_016855531.1:n.*86T>A
XM_024449826.1:c.682T>A	XP_024305594.1:p.Phe228Ile
XM_024449860.1:c.469T>A	XP_024305628.1:p.Phe157Ile
XM_024449871.1:c.469T>A	XP_024305639.1:p.Phe157Ile
NM_001378226.1:c.682T>A	NP_001365155.1:p.Phe228Ile
NM_001378227.1:c.682T>A	NP_001365156.1:p.Phe228Ile
NM_001378228.1:c.580T>A	NP_001365157.1:p.Phe194Ile
NM_001378229.1:c.493T>A	NP_001365158.1:p.Phe165Ile
NM_001378230.1:c.469T>A	NP_001365159.1:p.Phe157Ile
NM_001378231.1:c.*86T>A	NP_001365160.1:n.*86T>A
NM_015836.4:c.751T>A MANE Select	NP_056651.1:p.Phe251Ile