Canonical Allele Identifier: CA1192128197
Gene: WARS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.119033196_119033197delinsCG , CM000663.2:g.119033196_119033197delinsCG GRCh38
NC_000001.10:g.119575819_119575820delinsCG , CM000663.1:g.119575819_119575820delinsCG GRCh37
NC_000001.9:g.119377342_119377343delinsCG NCBI36
NG_050658.1:g.112592_112593delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000235521.5:c.797_798delinsCG MANE Select ENSP00000235521.4:p.Pro266=
ENST00000235521.4:c.797_798delinsCG ENSP00000235521.4:p.Pro266=
ENST00000369426.9:c.*163_*164delinsCG ENSP00000358434.5:n.*163_*164delinsCG
NM_015836.3:c.797_798delinsCG NP_056651.1:p.Pro266=
NM_201263.2:c.*163_*164delinsCG NP_957715.1:n.*163_*164delinsCG
XM_005270350.2:c.743_744delinsCG XP_005270407.1:p.Pro248=
XM_006710283.1:c.515_516delinsCG XP_006710346.1:p.Pro172=
XM_011540493.1:c.728_729delinsCG XP_011538795.1:p.Pro243=
XM_011540494.1:c.728_729delinsCG XP_011538796.1:p.Pro243=
XM_011540495.1:c.539_540delinsCG XP_011538797.1:p.Pro180=
XM_005270350.3:c.743_744delinsCG XP_005270407.1:p.Pro248=
XM_011540494.2:c.728_729delinsCG XP_011538796.1:p.Pro243=
XM_011540495.2:c.539_540delinsCG XP_011538797.1:p.Pro180=
XM_017000038.1:c.740_741delinsCG XP_016855527.1:p.Pro247=
XM_017000039.1:c.728_729delinsCG XP_016855528.1:p.Pro243=
XM_017000040.1:c.626_627delinsCG XP_016855529.1:p.Pro209=
XM_017000041.2:c.458_459delinsCG XP_016855530.1:p.Pro153=
XM_017000042.1:c.*132_*133delinsCG XP_016855531.1:n.*132_*133delinsCG
XM_024449826.1:c.728_729delinsCG XP_024305594.1:p.Pro243=
XM_024449860.1:c.515_516delinsCG XP_024305628.1:p.Pro172=
XM_024449871.1:c.515_516delinsCG XP_024305639.1:p.Pro172=
NM_001378226.1:c.728_729delinsCG NP_001365155.1:p.Pro243=
NM_001378227.1:c.728_729delinsCG NP_001365156.1:p.Pro243=
NM_001378228.1:c.626_627delinsCG NP_001365157.1:p.Pro209=
NM_001378229.1:c.539_540delinsCG NP_001365158.1:p.Pro180=
NM_001378230.1:c.515_516delinsCG NP_001365159.1:p.Pro172=
NM_001378231.1:c.*132_*133delinsCG NP_001365160.1:n.*132_*133delinsCG
NM_015836.4:c.797_798delinsCG MANE Select NP_056651.1:p.Pro266=