Canonical Allele Identifier: CA1984717759

Gene: NARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.78478605_78478606delinsAT , CM000673.2:g.78478605_78478606delinsAT	GRCh38
NC_000011.9:g.78189651_78189652delinsAT , CM000673.1:g.78189651_78189652delinsAT	GRCh37
NC_000011.8:g.77867299_77867300delinsAT	NCBI36
NG_042046.1:g.101259_101260delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525345.6:n.390_391delinsAT
ENST00000529771.2:c.219_220delinsAT	ENSP00000435298.2:p.Lys73=
ENST00000695114.1:n.3561_3562delinsAT
ENST00000695115.1:c.219_220delinsAT	ENSP00000511705.1:p.Lys73=
ENST00000695116.1:c.142-9293_142-9292delinsAT	ENSP00000511706.1:n.142-9293_142-9292delinsAT
ENST00000695341.1:c.*570_*571delinsAT	ENSP00000511816.1:n.*570_*571delinsAT
ENST00000695342.1:c.219_220delinsAT	ENSP00000511817.1:p.Lys73=
ENST00000695343.1:c.219_220delinsAT	ENSP00000511818.1:p.Lys73=
ENST00000695344.1:c.819_820delinsAT	ENSP00000511819.1:p.Lys273=
ENST00000695345.1:c.219_220delinsAT	ENSP00000511820.1:p.Lys73=
ENST00000695346.1:c.*317_*318delinsAT	ENSP00000511821.1:n.*317_*318delinsAT
ENST00000695347.1:c.*372_*373delinsAT	ENSP00000511822.1:n.*372_*373delinsAT
ENST00000695348.1:c.219_220delinsAT	ENSP00000511823.1:p.Lys73=
ENST00000695349.1:c.900_901delinsAT	ENSP00000511824.1:p.Lys300=
ENST00000695350.1:c.*71_*72delinsAT	ENSP00000511825.1:n.*71_*72delinsAT
ENST00000695351.1:c.823-12593_823-12592delinsAT	ENSP00000511826.1:n.823-12593_823-12592delinsAT
ENST00000695352.1:c.48_49delinsAT	ENSP00000511827.1:p.Lys16=
ENST00000695353.1:c.-105-12593_-105-12592delinsAT	ENSP00000511828.1:n.-105-12593_-105-12592delinsAT
ENST00000695354.1:c.900_901delinsAT	ENSP00000511829.1:p.Lys300=
ENST00000695355.1:c.900_901delinsAT	ENSP00000511830.1:p.Lys300=
ENST00000695356.1:c.*881_*882delinsAT	ENSP00000511831.1:n.*881_*882delinsAT
ENST00000695357.1:c.900_901delinsAT	ENSP00000511832.1:p.Lys300=
ENST00000695358.1:c.900_901delinsAT	ENSP00000511833.1:p.Lys300=
ENST00000695359.1:c.*557_*558delinsAT	ENSP00000511834.1:n.*557_*558delinsAT
ENST00000695360.1:c.900_901delinsAT	ENSP00000511835.1:p.Lys300=
ENST00000695361.1:c.*89-9293_*89-9292delinsAT	ENSP00000511836.1:n.*89-9293_*89-9292delinsAT
ENST00000695362.1:c.*220_*221delinsAT	ENSP00000511837.1:n.*220_*221delinsAT
ENST00000695364.1:n.1238_1239delinsAT
ENST00000695365.1:n.1190_1191delinsAT
ENST00000695366.1:c.900_901delinsAT	ENSP00000511838.1:p.Lys300=
ENST00000281038.10:c.900_901delinsAT MANE Select	ENSP00000281038.5:p.Lys300=
ENST00000281038.9:c.900_901delinsAT	ENSP00000281038.5:p.Lys300=
ENST00000525345.5:c.390_391delinsAT
ENST00000528850.5:c.219_220delinsAT	ENSP00000432635.1:p.Lys73=
ENST00000529880.1:c.595-12593_595-12592delinsAT	ENSP00000432240.1:n.595-12593_595-12592delinsAT
NM_001243251.1:c.219_220delinsAT	NP_001230180.1:p.Lys73=
NM_024678.5:c.900_901delinsAT	NP_078954.4:p.Lys300=
XM_011545253.1:c.900_901delinsAT	XP_011543555.1:p.Lys300=
XR_950050.1:n.1269_1270delinsAT
XR_950051.1:n.1269_1270delinsAT
XR_950344.1:n.199+3728_199+3729delinsAT
XR_950345.1:n.151+5309_151+5310delinsAT
XM_011545253.2:c.900_901delinsAT	XP_011543555.1:p.Lys300=
XM_017018302.2:c.900_901delinsAT	XP_016873791.1:p.Lys300=
XM_017018303.1:c.219_220delinsAT	XP_016873792.1:p.Lys73=
XM_017018304.2:c.219_220delinsAT	XP_016873793.1:p.Lys73=
XR_001747963.2:n.1254_1255delinsAT
XR_001747964.2:n.1254_1255delinsAT
XR_001747965.2:n.1254_1255delinsAT
XR_001747966.2:n.1254_1255delinsAT
XR_001748314.1:n.3035+3728_3035+3729delinsAT
NM_024678.6:c.900_901delinsAT MANE Select	NP_078954.4:p.Lys300=
NM_001243251.2:c.219_220delinsAT	NP_001230180.1:p.Lys73=