Canonical Allele Identifier: CA1984717778
Gene: NARS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.78478656T= , CM000673.2:g.78478656T= GRCh38
NC_000011.9:g.78189702T= , CM000673.1:g.78189702T= GRCh37
NC_000011.8:g.77867350T= NCBI36
NG_042046.1:g.101209A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525345.6:n.340A=
ENST00000529771.2:c.169A= ENSP00000435298.2:p.Thr57=
ENST00000695114.1:n.3511A=
ENST00000695115.1:c.169A= ENSP00000511705.1:p.Thr57=
ENST00000695116.1:c.142-9343A= ENSP00000511706.1:n.142-9343A=
ENST00000695341.1:c.*520A= ENSP00000511816.1:n.*520A=
ENST00000695342.1:c.169A= ENSP00000511817.1:p.Thr57=
ENST00000695343.1:c.169A= ENSP00000511818.1:p.Thr57=
ENST00000695344.1:c.769A= ENSP00000511819.1:p.Thr257=
ENST00000695345.1:c.169A= ENSP00000511820.1:p.Thr57=
ENST00000695346.1:c.*267A= ENSP00000511821.1:n.*267A=
ENST00000695347.1:c.*322A= ENSP00000511822.1:n.*322A=
ENST00000695348.1:c.169A= ENSP00000511823.1:p.Thr57=
ENST00000695349.1:c.850A= ENSP00000511824.1:p.Thr284=
ENST00000695350.1:c.*21A= ENSP00000511825.1:n.*21A=
ENST00000695351.1:c.823-12643A= ENSP00000511826.1:n.823-12643A=
ENST00000695352.1:c.-3A= ENSP00000511827.1:n.-3A=
ENST00000695353.1:c.-105-12643A= ENSP00000511828.1:n.-105-12643A=
ENST00000695354.1:c.850A= ENSP00000511829.1:p.Thr284=
ENST00000695355.1:c.850A= ENSP00000511830.1:p.Thr284=
ENST00000695356.1:c.*831A= ENSP00000511831.1:n.*831A=
ENST00000695357.1:c.850A= ENSP00000511832.1:p.Thr284=
ENST00000695358.1:c.850A= ENSP00000511833.1:p.Thr284=
ENST00000695359.1:c.*507A= ENSP00000511834.1:n.*507A=
ENST00000695360.1:c.850A= ENSP00000511835.1:p.Thr284=
ENST00000695361.1:c.*89-9343A= ENSP00000511836.1:n.*89-9343A=
ENST00000695362.1:c.*170A= ENSP00000511837.1:n.*170A=
ENST00000695364.1:n.1188A=
ENST00000695365.1:n.1140A=
ENST00000695366.1:c.850A= ENSP00000511838.1:p.Thr284=
ENST00000281038.10:c.850A= MANE Select ENSP00000281038.5:p.Thr284=
ENST00000281038.9:c.850A= ENSP00000281038.5:p.Thr284=
ENST00000525345.5:c.340A=
ENST00000528850.5:c.169A= ENSP00000432635.1:p.Thr57=
ENST00000529880.1:c.595-12643A= ENSP00000432240.1:n.595-12643A=
NM_001243251.1:c.169A= NP_001230180.1:p.Thr57=
NM_024678.5:c.850A= NP_078954.4:p.Thr284=
XM_011545253.1:c.850A= XP_011543555.1:p.Thr284=
XR_950050.1:n.1219A=
XR_950051.1:n.1219A=
XR_950344.1:n.199+3779T=
XR_950345.1:n.151+5360T=
XM_011545253.2:c.850A= XP_011543555.1:p.Thr284=
XM_017018302.2:c.850A= XP_016873791.1:p.Thr284=
XM_017018303.1:c.169A= XP_016873792.1:p.Thr57=
XM_017018304.2:c.169A= XP_016873793.1:p.Thr57=
XR_001747963.2:n.1204A=
XR_001747964.2:n.1204A=
XR_001747965.2:n.1204A=
XR_001747966.2:n.1204A=
XR_001748314.1:n.3035+3779T=
NM_024678.6:c.850A= MANE Select NP_078954.4:p.Thr284=
NM_001243251.2:c.169A= NP_001230180.1:p.Thr57=