Canonical Allele Identifier: CA341436723

Gene: WARS2

Linked Data

• MyVariant Identifiers: chr1:g.119575877A>T (hg19) ; chr1:g.119033254A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119033254A>T , CM000663.2:g.119033254A>T	GRCh38
NC_000001.10:g.119575877A>T , CM000663.1:g.119575877A>T	GRCh37
NC_000001.9:g.119377400A>T	NCBI36
NG_050658.1:g.112535T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235521.5:c.740T>A MANE Select	ENSP00000235521.4:p.Ile247Lys
ENST00000235521.4:c.740T>A	ENSP00000235521.4:p.Ile247Lys
ENST00000369426.9:c.*106T>A	ENSP00000358434.5:n.*106T>A
NM_015836.3:c.740T>A	NP_056651.1:p.Ile247Lys
NM_201263.2:c.*106T>A	NP_957715.1:n.*106T>A
XM_005270350.2:c.686T>A	XP_005270407.1:p.Ile229Lys
XM_006710283.1:c.458T>A	XP_006710346.1:p.Ile153Lys
XM_011540493.1:c.671T>A	XP_011538795.1:p.Ile224Lys
XM_011540494.1:c.671T>A	XP_011538796.1:p.Ile224Lys
XM_011540495.1:c.482T>A	XP_011538797.1:p.Ile161Lys
XM_005270350.3:c.686T>A	XP_005270407.1:p.Ile229Lys
XM_011540494.2:c.671T>A	XP_011538796.1:p.Ile224Lys
XM_011540495.2:c.482T>A	XP_011538797.1:p.Ile161Lys
XM_017000038.1:c.683T>A	XP_016855527.1:p.Ile228Lys
XM_017000039.1:c.671T>A	XP_016855528.1:p.Ile224Lys
XM_017000040.1:c.569T>A	XP_016855529.1:p.Ile190Lys
XM_017000041.2:c.401T>A	XP_016855530.1:p.Ile134Lys
XM_017000042.1:c.*75T>A	XP_016855531.1:n.*75T>A
XM_024449826.1:c.671T>A	XP_024305594.1:p.Ile224Lys
XM_024449860.1:c.458T>A	XP_024305628.1:p.Ile153Lys
XM_024449871.1:c.458T>A	XP_024305639.1:p.Ile153Lys
NM_001378226.1:c.671T>A	NP_001365155.1:p.Ile224Lys
NM_001378227.1:c.671T>A	NP_001365156.1:p.Ile224Lys
NM_001378228.1:c.569T>A	NP_001365157.1:p.Ile190Lys
NM_001378229.1:c.482T>A	NP_001365158.1:p.Ile161Lys
NM_001378230.1:c.458T>A	NP_001365159.1:p.Ile153Lys
NM_001378231.1:c.*75T>A	NP_001365160.1:n.*75T>A
NM_015836.4:c.740T>A MANE Select	NP_056651.1:p.Ile247Lys