Canonical Allele Identifier: CA1984717776

Gene: NARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.78478652_78478655delinsATTG , CM000673.2:g.78478652_78478655delinsATTG	GRCh38
NC_000011.9:g.78189698_78189701delinsATTG , CM000673.1:g.78189698_78189701delinsATTG	GRCh37
NC_000011.8:g.77867346_77867349delinsATTG	NCBI36
NG_042046.1:g.101210_101213delinsCAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525345.6:n.341_344delinsCAAT
ENST00000529771.2:c.170_173delinsCAAT	ENSP00000435298.2:p.Thr57=
ENST00000695114.1:n.3512_3515delinsCAAT
ENST00000695115.1:c.170_173delinsCAAT	ENSP00000511705.1:p.Thr57=
ENST00000695116.1:c.142-9342_142-9339delinsCAAT	ENSP00000511706.1:n.142-9342_142-9339delinsCAAT
ENST00000695341.1:c.*521_*524delinsCAAT	ENSP00000511816.1:n.*521_*524delinsCAAT
ENST00000695342.1:c.170_173delinsCAAT	ENSP00000511817.1:p.Thr57=
ENST00000695343.1:c.170_173delinsCAAT	ENSP00000511818.1:p.Thr57=
ENST00000695344.1:c.770_773delinsCAAT	ENSP00000511819.1:p.Thr257=
ENST00000695345.1:c.170_173delinsCAAT	ENSP00000511820.1:p.Thr57=
ENST00000695346.1:c.*268_*271delinsCAAT	ENSP00000511821.1:n.*268_*271delinsCAAT
ENST00000695347.1:c.*323_*326delinsCAAT	ENSP00000511822.1:n.*323_*326delinsCAAT
ENST00000695348.1:c.170_173delinsCAAT	ENSP00000511823.1:p.Thr57=
ENST00000695349.1:c.851_854delinsCAAT	ENSP00000511824.1:p.Thr284=
ENST00000695350.1:c.*22_*25delinsCAAT	ENSP00000511825.1:n.*22_*25delinsCAAT
ENST00000695351.1:c.823-12642_823-12639delinsCAAT	ENSP00000511826.1:n.823-12642_823-12639delinsCAAT
ENST00000695352.1:c.-2_2delinsCAAT
ENST00000695353.1:c.-105-12642_-105-12639delinsCAAT	ENSP00000511828.1:n.-105-12642_-105-12639delinsCAAT
ENST00000695354.1:c.851_854delinsCAAT	ENSP00000511829.1:p.Thr284=
ENST00000695355.1:c.851_854delinsCAAT	ENSP00000511830.1:p.Thr284=
ENST00000695356.1:c.*832_*835delinsCAAT	ENSP00000511831.1:n.*832_*835delinsCAAT
ENST00000695357.1:c.851_854delinsCAAT	ENSP00000511832.1:p.Thr284=
ENST00000695358.1:c.851_854delinsCAAT	ENSP00000511833.1:p.Thr284=
ENST00000695359.1:c.*508_*511delinsCAAT	ENSP00000511834.1:n.*508_*511delinsCAAT
ENST00000695360.1:c.851_854delinsCAAT	ENSP00000511835.1:p.Thr284=
ENST00000695361.1:c.*89-9342_*89-9339delinsCAAT	ENSP00000511836.1:n.*89-9342_*89-9339delinsCAAT
ENST00000695362.1:c.*171_*174delinsCAAT	ENSP00000511837.1:n.*171_*174delinsCAAT
ENST00000695364.1:n.1189_1192delinsCAAT
ENST00000695365.1:n.1141_1144delinsCAAT
ENST00000695366.1:c.851_854delinsCAAT	ENSP00000511838.1:p.Thr284=
ENST00000281038.10:c.851_854delinsCAAT MANE Select	ENSP00000281038.5:p.Thr284=
ENST00000281038.9:c.851_854delinsCAAT	ENSP00000281038.5:p.Thr284=
ENST00000525345.5:c.341_344delinsCAAT
ENST00000528850.5:c.170_173delinsCAAT	ENSP00000432635.1:p.Thr57=
ENST00000529880.1:c.595-12642_595-12639delinsCAAT	ENSP00000432240.1:n.595-12642_595-12639delinsCAAT
NM_001243251.1:c.170_173delinsCAAT	NP_001230180.1:p.Thr57=
NM_024678.5:c.851_854delinsCAAT	NP_078954.4:p.Thr284=
XM_011545253.1:c.851_854delinsCAAT	XP_011543555.1:p.Thr284=
XR_950050.1:n.1220_1223delinsCAAT
XR_950051.1:n.1220_1223delinsCAAT
XR_950344.1:n.199+3775_199+3778delinsATTG
XR_950345.1:n.151+5356_151+5359delinsATTG
XM_011545253.2:c.851_854delinsCAAT	XP_011543555.1:p.Thr284=
XM_017018302.2:c.851_854delinsCAAT	XP_016873791.1:p.Thr284=
XM_017018303.1:c.170_173delinsCAAT	XP_016873792.1:p.Thr57=
XM_017018304.2:c.170_173delinsCAAT	XP_016873793.1:p.Thr57=
XR_001747963.2:n.1205_1208delinsCAAT
XR_001747964.2:n.1205_1208delinsCAAT
XR_001747965.2:n.1205_1208delinsCAAT
XR_001747966.2:n.1205_1208delinsCAAT
XR_001748314.1:n.3035+3775_3035+3778delinsATTG
NM_024678.6:c.851_854delinsCAAT MANE Select	NP_078954.4:p.Thr284=
NM_001243251.2:c.170_173delinsCAAT	NP_001230180.1:p.Thr57=