Canonical Allele Identifier: CA341436523

Gene: WARS2

Linked Data

• MyVariant Identifiers: chr1:g.119575780A>C (hg19) ; chr1:g.119033157A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119033157A>C , CM000663.2:g.119033157A>C	GRCh38
NC_000001.10:g.119575780A>C , CM000663.1:g.119575780A>C	GRCh37
NC_000001.9:g.119377303A>C	NCBI36
NG_050658.1:g.112632T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235521.5:c.837T>G MANE Select	ENSP00000235521.4:p.His279Gln
ENST00000235521.4:c.837T>G	ENSP00000235521.4:p.His279Gln
ENST00000369426.9:c.*203T>G	ENSP00000358434.5:n.*203T>G
NM_015836.3:c.837T>G	NP_056651.1:p.His279Gln
NM_201263.2:c.*203T>G	NP_957715.1:n.*203T>G
XM_005270350.2:c.783T>G	XP_005270407.1:p.His261Gln
XM_006710283.1:c.555T>G	XP_006710346.1:p.His185Gln
XM_011540493.1:c.768T>G	XP_011538795.1:p.His256Gln
XM_011540494.1:c.768T>G	XP_011538796.1:p.His256Gln
XM_011540495.1:c.579T>G	XP_011538797.1:p.His193Gln
XM_005270350.3:c.783T>G	XP_005270407.1:p.His261Gln
XM_011540494.2:c.768T>G	XP_011538796.1:p.His256Gln
XM_011540495.2:c.579T>G	XP_011538797.1:p.His193Gln
XM_017000038.1:c.780T>G	XP_016855527.1:p.His260Gln
XM_017000039.1:c.768T>G	XP_016855528.1:p.His256Gln
XM_017000040.1:c.666T>G	XP_016855529.1:p.His222Gln
XM_017000041.2:c.498T>G	XP_016855530.1:p.His166Gln
XM_017000042.1:c.*172T>G	XP_016855531.1:n.*172T>G
XM_024449826.1:c.768T>G	XP_024305594.1:p.His256Gln
XM_024449860.1:c.555T>G	XP_024305628.1:p.His185Gln
XM_024449871.1:c.555T>G	XP_024305639.1:p.His185Gln
NM_001378226.1:c.768T>G	NP_001365155.1:p.His256Gln
NM_001378227.1:c.768T>G	NP_001365156.1:p.His256Gln
NM_001378228.1:c.666T>G	NP_001365157.1:p.His222Gln
NM_001378229.1:c.579T>G	NP_001365158.1:p.His193Gln
NM_001378230.1:c.555T>G	NP_001365159.1:p.His185Gln
NM_001378231.1:c.*172T>G	NP_001365160.1:n.*172T>G
NM_015836.4:c.837T>G MANE Select	NP_056651.1:p.His279Gln