Canonical Allele Identifier: CA341436641

Gene: WARS2

Linked Data

• MyVariant Identifiers: chr1:g.119575841G>T (hg19) ; chr1:g.119033218G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119033218G>T , CM000663.2:g.119033218G>T	GRCh38
NC_000001.10:g.119575841G>T , CM000663.1:g.119575841G>T	GRCh37
NC_000001.9:g.119377364G>T	NCBI36
NG_050658.1:g.112571C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235521.5:c.776C>A MANE Select	ENSP00000235521.4:p.Thr259Asn
ENST00000235521.4:c.776C>A	ENSP00000235521.4:p.Thr259Asn
ENST00000369426.9:c.*142C>A	ENSP00000358434.5:n.*142C>A
NM_015836.3:c.776C>A	NP_056651.1:p.Thr259Asn
NM_201263.2:c.*142C>A	NP_957715.1:n.*142C>A
XM_005270350.2:c.722C>A	XP_005270407.1:p.Thr241Asn
XM_006710283.1:c.494C>A	XP_006710346.1:p.Thr165Asn
XM_011540493.1:c.707C>A	XP_011538795.1:p.Thr236Asn
XM_011540494.1:c.707C>A	XP_011538796.1:p.Thr236Asn
XM_011540495.1:c.518C>A	XP_011538797.1:p.Thr173Asn
XM_005270350.3:c.722C>A	XP_005270407.1:p.Thr241Asn
XM_011540494.2:c.707C>A	XP_011538796.1:p.Thr236Asn
XM_011540495.2:c.518C>A	XP_011538797.1:p.Thr173Asn
XM_017000038.1:c.719C>A	XP_016855527.1:p.Thr240Asn
XM_017000039.1:c.707C>A	XP_016855528.1:p.Thr236Asn
XM_017000040.1:c.605C>A	XP_016855529.1:p.Thr202Asn
XM_017000041.2:c.437C>A	XP_016855530.1:p.Thr146Asn
XM_017000042.1:c.*111C>A	XP_016855531.1:n.*111C>A
XM_024449826.1:c.707C>A	XP_024305594.1:p.Thr236Asn
XM_024449860.1:c.494C>A	XP_024305628.1:p.Thr165Asn
XM_024449871.1:c.494C>A	XP_024305639.1:p.Thr165Asn
NM_001378226.1:c.707C>A	NP_001365155.1:p.Thr236Asn
NM_001378227.1:c.707C>A	NP_001365156.1:p.Thr236Asn
NM_001378228.1:c.605C>A	NP_001365157.1:p.Thr202Asn
NM_001378229.1:c.518C>A	NP_001365158.1:p.Thr173Asn
NM_001378230.1:c.494C>A	NP_001365159.1:p.Thr165Asn
NM_001378231.1:c.*111C>A	NP_001365160.1:n.*111C>A
NM_015836.4:c.776C>A MANE Select	NP_056651.1:p.Thr259Asn