Canonical Allele Identifier: CA1192170775

Gene: WARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119140361_119140362delinsCT , CM000663.2:g.119140361_119140362delinsCT	GRCh38
NC_000001.10:g.119682984_119682985delinsCT , CM000663.1:g.119682984_119682985delinsCT	GRCh37
NC_000001.9:g.119484507_119484508delinsCT	NCBI36
NG_050658.1:g.5427_5428delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235521.5:c.90+193_90+194delinsAG MANE Select	ENSP00000235521.4:n.90+193_90+194delinsAG
ENST00000235521.4:c.90+193_90+194delinsAG	ENSP00000235521.4:n.90+193_90+194delinsAG
ENST00000369426.9:c.90+193_90+194delinsAG	ENSP00000358434.5:n.90+193_90+194delinsAG
ENST00000495746.5:n.100+193_100+194delinsAG
ENST00000497761.1:n.181_182delinsAG
NM_015836.3:c.90+193_90+194delinsAG	NP_056651.1:n.90+193_90+194delinsAG
NM_201263.2:c.90+193_90+194delinsAG	NP_957715.1:n.90+193_90+194delinsAG
XM_006710283.1:c.-287_-286delinsAG	XP_006710346.1:n.-287_-286delinsAG
XM_011540493.1:c.-159_-158delinsAG	XP_011538795.1:n.-159_-158delinsAG
XM_011540494.1:c.-65+193_-65+194delinsAG	XP_011538796.1:n.-65+193_-65+194delinsAG
XM_011540495.1:c.90+193_90+194delinsAG	XP_011538797.1:n.90+193_90+194delinsAG
XM_011540494.2:c.-65+193_-65+194delinsAG	XP_011538796.1:n.-65+193_-65+194delinsAG
XM_011540495.2:c.90+193_90+194delinsAG	XP_011538797.1:n.90+193_90+194delinsAG
XM_017000038.1:c.90+193_90+194delinsAG	XP_016855527.1:n.90+193_90+194delinsAG
XM_017000039.1:c.-159_-158delinsAG	XP_016855528.1:n.-159_-158delinsAG
XM_017000040.1:c.90+193_90+194delinsAG	XP_016855529.1:n.90+193_90+194delinsAG
XM_017000041.2:c.-287_-286delinsAG	XP_016855530.1:n.-287_-286delinsAG
XM_017000042.1:c.90+193_90+194delinsAG	XP_016855531.1:n.90+193_90+194delinsAG
XM_024449826.1:c.-159_-158delinsAG	XP_024305594.1:n.-159_-158delinsAG
XM_024449860.1:c.-287_-286delinsAG	XP_024305628.1:n.-287_-286delinsAG
XM_024449871.1:c.-287_-286delinsAG	XP_024305639.1:n.-287_-286delinsAG
NM_001378226.1:c.-65+193_-65+194delinsAG	NP_001365155.1:n.-65+193_-65+194delinsAG
NM_001378227.1:c.-159_-158delinsAG	NP_001365156.1:n.-159_-158delinsAG
NM_001378228.1:c.90+193_90+194delinsAG	NP_001365157.1:n.90+193_90+194delinsAG
NM_001378229.1:c.90+193_90+194delinsAG	NP_001365158.1:n.90+193_90+194delinsAG
NM_001378230.1:c.-287_-286delinsAG	NP_001365159.1:n.-287_-286delinsAG
NM_001378231.1:c.90+193_90+194delinsAG	NP_001365160.1:n.90+193_90+194delinsAG
NM_015836.4:c.90+193_90+194delinsAG MANE Select	NP_056651.1:n.90+193_90+194delinsAG