Canonical Allele Identifier: CA2647370034

Gene: WARS2

Linked Data

• gnomAD v4: 1-119033174-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119033176del , CM000663.2:g.119033176del	GRCh38
NC_000001.10:g.119575799del , CM000663.1:g.119575799del	GRCh37
NC_000001.9:g.119377322del	NCBI36
NG_050658.1:g.112614del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235521.5:c.819del MANE Select	ENSP00000235521.4:p.Asn274ThrfsTer2
ENST00000235521.4:c.819del	ENSP00000235521.4:p.Asn274ThrfsTer2
ENST00000369426.9:c.*185del	ENSP00000358434.5:n.*185del
NM_015836.3:c.819del	NP_056651.1:p.Asn274ThrfsTer2
NM_201263.2:c.*185del	NP_957715.1:n.*185del
XM_005270350.2:c.765del	XP_005270407.1:p.Asn256ThrfsTer2
XM_006710283.1:c.537del	XP_006710346.1:p.Asn180ThrfsTer2
XM_011540493.1:c.750del	XP_011538795.1:p.Asn251ThrfsTer2
XM_011540494.1:c.750del	XP_011538796.1:p.Asn251ThrfsTer2
XM_011540495.1:c.561del	XP_011538797.1:p.Asn188ThrfsTer2
XM_005270350.3:c.765del	XP_005270407.1:p.Asn256ThrfsTer2
XM_011540494.2:c.750del	XP_011538796.1:p.Asn251ThrfsTer2
XM_011540495.2:c.561del	XP_011538797.1:p.Asn188ThrfsTer2
XM_017000038.1:c.762del	XP_016855527.1:p.Asn255ThrfsTer2
XM_017000039.1:c.750del	XP_016855528.1:p.Asn251ThrfsTer2
XM_017000040.1:c.648del	XP_016855529.1:p.Asn217ThrfsTer2
XM_017000041.2:c.480del	XP_016855530.1:p.Asn161ThrfsTer2
XM_017000042.1:c.*154del	XP_016855531.1:n.*154del
XM_024449826.1:c.750del	XP_024305594.1:p.Asn251ThrfsTer2
XM_024449860.1:c.537del	XP_024305628.1:p.Asn180ThrfsTer2
XM_024449871.1:c.537del	XP_024305639.1:p.Asn180ThrfsTer2
NM_001378226.1:c.750del	NP_001365155.1:p.Asn251ThrfsTer2
NM_001378227.1:c.750del	NP_001365156.1:p.Asn251ThrfsTer2
NM_001378228.1:c.648del	NP_001365157.1:p.Asn217ThrfsTer2
NM_001378229.1:c.561del	NP_001365158.1:p.Asn188ThrfsTer2
NM_001378230.1:c.537del	NP_001365159.1:p.Asn180ThrfsTer2
NM_001378231.1:c.*154del	NP_001365160.1:n.*154del
NM_015836.4:c.819del MANE Select	NP_056651.1:p.Asn274ThrfsTer2