Canonical Allele Identifier: CA420192757

Gene: WARS2

Linked Data

• MyVariant Identifiers: chr1:g.119575855A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119033232A>C , CM000663.2:g.119033232A>C	GRCh38
NC_000001.10:g.119575855A>C , CM000663.1:g.119575855A>C	GRCh37
NC_000001.9:g.119377378A>C	NCBI36
NG_050658.1:g.112557T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235521.5:c.762T>G MANE Select	ENSP00000235521.4:p.Ala254=
ENST00000235521.4:c.762T>G	ENSP00000235521.4:p.Ala254=
ENST00000369426.9:c.*128T>G	ENSP00000358434.5:n.*128T>G
NM_015836.3:c.762T>G	NP_056651.1:p.Ala254=
NM_201263.2:c.*128T>G	NP_957715.1:n.*128T>G
XM_005270350.2:c.708T>G	XP_005270407.1:p.Ala236=
XM_006710283.1:c.480T>G	XP_006710346.1:p.Ala160=
XM_011540493.1:c.693T>G	XP_011538795.1:p.Ala231=
XM_011540494.1:c.693T>G	XP_011538796.1:p.Ala231=
XM_011540495.1:c.504T>G	XP_011538797.1:p.Ala168=
XM_005270350.3:c.708T>G	XP_005270407.1:p.Ala236=
XM_011540494.2:c.693T>G	XP_011538796.1:p.Ala231=
XM_011540495.2:c.504T>G	XP_011538797.1:p.Ala168=
XM_017000038.1:c.705T>G	XP_016855527.1:p.Ala235=
XM_017000039.1:c.693T>G	XP_016855528.1:p.Ala231=
XM_017000040.1:c.591T>G	XP_016855529.1:p.Ala197=
XM_017000041.2:c.423T>G	XP_016855530.1:p.Ala141=
XM_017000042.1:c.*97T>G	XP_016855531.1:n.*97T>G
XM_024449826.1:c.693T>G	XP_024305594.1:p.Ala231=
XM_024449860.1:c.480T>G	XP_024305628.1:p.Ala160=
XM_024449871.1:c.480T>G	XP_024305639.1:p.Ala160=
NM_001378226.1:c.693T>G	NP_001365155.1:p.Ala231=
NM_001378227.1:c.693T>G	NP_001365156.1:p.Ala231=
NM_001378228.1:c.591T>G	NP_001365157.1:p.Ala197=
NM_001378229.1:c.504T>G	NP_001365158.1:p.Ala168=
NM_001378230.1:c.480T>G	NP_001365159.1:p.Ala160=
NM_001378231.1:c.*97T>G	NP_001365160.1:n.*97T>G
NM_015836.4:c.762T>G MANE Select	NP_056651.1:p.Ala254=