Canonical Allele Identifier: CA2615327784

Gene: NARS2

Linked Data

• gnomAD v4: 11-78478585-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.78478589del , CM000673.2:g.78478589del	GRCh38
NC_000011.9:g.78189635del , CM000673.1:g.78189635del	GRCh37
NC_000011.8:g.77867283del	NCBI36
NG_042046.1:g.101279del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525345.6:n.410del
ENST00000529771.2:c.239del	ENSP00000435298.2:p.Lys80ArgfsTer4
ENST00000695114.1:n.3581del
ENST00000695115.1:c.239del	ENSP00000511705.1:p.Lys80ArgfsTer4
ENST00000695116.1:c.142-9273del	ENSP00000511706.1:n.142-9273del
ENST00000695341.1:c.*590del	ENSP00000511816.1:n.*590del
ENST00000695342.1:c.239del	ENSP00000511817.1:p.Lys80ArgfsTer4
ENST00000695343.1:c.239del	ENSP00000511818.1:p.Lys80ArgfsTer4
ENST00000695344.1:c.839del	ENSP00000511819.1:p.Lys280ArgfsTer4
ENST00000695345.1:c.239del	ENSP00000511820.1:p.Lys80ArgfsTer4
ENST00000695346.1:c.*337del	ENSP00000511821.1:n.*337del
ENST00000695347.1:c.*392del	ENSP00000511822.1:n.*392del
ENST00000695348.1:c.239del	ENSP00000511823.1:p.Lys80ArgfsTer4
ENST00000695349.1:c.920del	ENSP00000511824.1:p.Lys307ArgfsTer4
ENST00000695350.1:c.*91del	ENSP00000511825.1:n.*91del
ENST00000695351.1:c.823-12573del	ENSP00000511826.1:n.823-12573del
ENST00000695352.1:c.68del	ENSP00000511827.1:p.Lys23ArgfsTer4
ENST00000695353.1:c.-105-12573del	ENSP00000511828.1:n.-105-12573del
ENST00000695354.1:c.920del	ENSP00000511829.1:p.Lys307ArgfsTer4
ENST00000695355.1:c.920del	ENSP00000511830.1:p.Lys307ArgfsTer4
ENST00000695356.1:c.*901del	ENSP00000511831.1:n.*901del
ENST00000695357.1:c.920del	ENSP00000511832.1:p.Lys307ArgfsTer4
ENST00000695358.1:c.920del	ENSP00000511833.1:p.Lys307ArgfsTer4
ENST00000695359.1:c.*577del	ENSP00000511834.1:n.*577del
ENST00000695360.1:c.920del	ENSP00000511835.1:p.Lys307ArgfsTer4
ENST00000695361.1:c.*89-9273del	ENSP00000511836.1:n.*89-9273del
ENST00000695362.1:c.*240del	ENSP00000511837.1:n.*240del
ENST00000695364.1:n.1258del
ENST00000695365.1:n.1210del
ENST00000695366.1:c.920del	ENSP00000511838.1:p.Lys307ArgfsTer4
ENST00000281038.10:c.920del MANE Select	ENSP00000281038.5:p.Lys307ArgfsTer4
ENST00000281038.9:c.920del	ENSP00000281038.5:p.Lys307ArgfsTer4
ENST00000525345.5:c.410del
ENST00000528850.5:c.239del	ENSP00000432635.1:p.Lys80ArgfsTer4
ENST00000529880.1:c.595-12573del	ENSP00000432240.1:n.595-12573del
NM_001243251.1:c.239del	NP_001230180.1:p.Lys80ArgfsTer4
NM_024678.5:c.920del	NP_078954.4:p.Lys307ArgfsTer4
XM_011545253.1:c.920del	XP_011543555.1:p.Lys307ArgfsTer4
XR_950050.1:n.1289del
XR_950051.1:n.1289del
XR_950344.1:n.199+3712del
XR_950345.1:n.151+5293del
XM_011545253.2:c.920del	XP_011543555.1:p.Lys307ArgfsTer4
XM_017018302.2:c.920del	XP_016873791.1:p.Lys307SerfsTer?
XM_017018303.1:c.239del	XP_016873792.1:p.Lys80ArgfsTer4
XM_017018304.2:c.239del	XP_016873793.1:p.Lys80ArgfsTer4
XR_001747963.2:n.1274del
XR_001747964.2:n.1274del
XR_001747965.2:n.1274del
XR_001747966.2:n.1274del
XR_001748314.1:n.3035+3712del
NM_024678.6:c.920del MANE Select	NP_078954.4:p.Lys307ArgfsTer4
NM_001243251.2:c.239del	NP_001230180.1:p.Lys80ArgfsTer4