Canonical Allele Identifier: CA341436805

Gene: WARS2

Linked Data

• MyVariant Identifiers: chr1:g.119575916T>G (hg19) ; chr1:g.119033293T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119033293T>G , CM000663.2:g.119033293T>G	GRCh38
NC_000001.10:g.119575916T>G , CM000663.1:g.119575916T>G	GRCh37
NC_000001.9:g.119377439T>G	NCBI36
NG_050658.1:g.112496A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235521.5:c.701A>C MANE Select	ENSP00000235521.4:p.Lys234Thr
ENST00000235521.4:c.701A>C	ENSP00000235521.4:p.Lys234Thr
ENST00000369426.9:c.*67A>C	ENSP00000358434.5:n.*67A>C
NM_015836.3:c.701A>C	NP_056651.1:p.Lys234Thr
NM_201263.2:c.*67A>C	NP_957715.1:n.*67A>C
XM_005270350.2:c.647A>C	XP_005270407.1:p.Lys216Thr
XM_006710283.1:c.419A>C	XP_006710346.1:p.Lys140Thr
XM_011540493.1:c.632A>C	XP_011538795.1:p.Lys211Thr
XM_011540494.1:c.632A>C	XP_011538796.1:p.Lys211Thr
XM_011540495.1:c.443A>C	XP_011538797.1:p.Lys148Thr
XM_005270350.3:c.647A>C	XP_005270407.1:p.Lys216Thr
XM_011540494.2:c.632A>C	XP_011538796.1:p.Lys211Thr
XM_011540495.2:c.443A>C	XP_011538797.1:p.Lys148Thr
XM_017000038.1:c.644A>C	XP_016855527.1:p.Lys215Thr
XM_017000039.1:c.632A>C	XP_016855528.1:p.Lys211Thr
XM_017000040.1:c.530A>C	XP_016855529.1:p.Lys177Thr
XM_017000041.2:c.362A>C	XP_016855530.1:p.Lys121Thr
XM_017000042.1:c.*36A>C	XP_016855531.1:n.*36A>C
XM_024449826.1:c.632A>C	XP_024305594.1:p.Lys211Thr
XM_024449860.1:c.419A>C	XP_024305628.1:p.Lys140Thr
XM_024449871.1:c.419A>C	XP_024305639.1:p.Lys140Thr
NM_001378226.1:c.632A>C	NP_001365155.1:p.Lys211Thr
NM_001378227.1:c.632A>C	NP_001365156.1:p.Lys211Thr
NM_001378228.1:c.530A>C	NP_001365157.1:p.Lys177Thr
NM_001378229.1:c.443A>C	NP_001365158.1:p.Lys148Thr
NM_001378230.1:c.419A>C	NP_001365159.1:p.Lys140Thr
NM_001378231.1:c.*36A>C	NP_001365160.1:n.*36A>C
NM_015836.4:c.701A>C MANE Select	NP_056651.1:p.Lys234Thr