Canonical Allele Identifier: CA341436496

Gene: WARS2

Linked Data

• MyVariant Identifiers: chr1:g.119575766C>A (hg19) ; chr1:g.119033143C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119033143C>A , CM000663.2:g.119033143C>A	GRCh38
NC_000001.10:g.119575766C>A , CM000663.1:g.119575766C>A	GRCh37
NC_000001.9:g.119377289C>A	NCBI36
NG_050658.1:g.112646G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235521.5:c.851G>T MANE Select	ENSP00000235521.4:p.Gly284Val
ENST00000235521.4:c.851G>T	ENSP00000235521.4:p.Gly284Val
ENST00000369426.9:c.*217G>T	ENSP00000358434.5:n.*217G>T
NM_015836.3:c.851G>T	NP_056651.1:p.Gly284Val
NM_201263.2:c.*217G>T	NP_957715.1:n.*217G>T
XM_005270350.2:c.797G>T	XP_005270407.1:p.Gly266Val
XM_006710283.1:c.569G>T	XP_006710346.1:p.Gly190Val
XM_011540493.1:c.782G>T	XP_011538795.1:p.Gly261Val
XM_011540494.1:c.782G>T	XP_011538796.1:p.Gly261Val
XM_011540495.1:c.593G>T	XP_011538797.1:p.Gly198Val
XM_005270350.3:c.797G>T	XP_005270407.1:p.Gly266Val
XM_011540494.2:c.782G>T	XP_011538796.1:p.Gly261Val
XM_011540495.2:c.593G>T	XP_011538797.1:p.Gly198Val
XM_017000038.1:c.794G>T	XP_016855527.1:p.Gly265Val
XM_017000039.1:c.782G>T	XP_016855528.1:p.Gly261Val
XM_017000040.1:c.680G>T	XP_016855529.1:p.Gly227Val
XM_017000041.2:c.512G>T	XP_016855530.1:p.Gly171Val
XM_017000042.1:c.*186G>T	XP_016855531.1:n.*186G>T
XM_024449826.1:c.782G>T	XP_024305594.1:p.Gly261Val
XM_024449860.1:c.569G>T	XP_024305628.1:p.Gly190Val
XM_024449871.1:c.569G>T	XP_024305639.1:p.Gly190Val
NM_001378226.1:c.782G>T	NP_001365155.1:p.Gly261Val
NM_001378227.1:c.782G>T	NP_001365156.1:p.Gly261Val
NM_001378228.1:c.680G>T	NP_001365157.1:p.Gly227Val
NM_001378229.1:c.593G>T	NP_001365158.1:p.Gly198Val
NM_001378230.1:c.569G>T	NP_001365159.1:p.Gly190Val
NM_001378231.1:c.*186G>T	NP_001365160.1:n.*186G>T
NM_015836.4:c.851G>T MANE Select	NP_056651.1:p.Gly284Val