Canonical Allele Identifier: CA2615327785

Gene: NARS2

Linked Data

• gnomAD v4: 11-78478651-CATT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.78478652_78478654del , CM000673.2:g.78478652_78478654del	GRCh38
NC_000011.9:g.78189698_78189700del , CM000673.1:g.78189698_78189700del	GRCh37
NC_000011.8:g.77867346_77867348del	NCBI36
NG_042046.1:g.101211_101213del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525345.6:n.342_344del
ENST00000529771.2:c.171_173del	ENSP00000435298.2:p.Met58del
ENST00000695114.1:n.3513_3515del
ENST00000695115.1:c.171_173del	ENSP00000511705.1:p.Met58del
ENST00000695116.1:c.142-9341_142-9339del	ENSP00000511706.1:n.142-9341_142-9339del
ENST00000695341.1:c.*522_*524del	ENSP00000511816.1:n.*522_*524del
ENST00000695342.1:c.171_173del	ENSP00000511817.1:p.Met58del
ENST00000695343.1:c.171_173del	ENSP00000511818.1:p.Met58del
ENST00000695344.1:c.771_773del	ENSP00000511819.1:p.Met258del
ENST00000695345.1:c.171_173del	ENSP00000511820.1:p.Met58del
ENST00000695346.1:c.*269_*271del	ENSP00000511821.1:n.*269_*271del
ENST00000695347.1:c.*324_*326del	ENSP00000511822.1:n.*324_*326del
ENST00000695348.1:c.171_173del	ENSP00000511823.1:p.Met58del
ENST00000695349.1:c.852_854del	ENSP00000511824.1:p.Met285del
ENST00000695350.1:c.*23_*25del	ENSP00000511825.1:n.*23_*25del
ENST00000695351.1:c.823-12641_823-12639del	ENSP00000511826.1:n.823-12641_823-12639del
ENST00000695352.1:c.-1_2del
ENST00000695353.1:c.-105-12641_-105-12639del	ENSP00000511828.1:n.-105-12641_-105-12639del
ENST00000695354.1:c.852_854del	ENSP00000511829.1:p.Met285del
ENST00000695355.1:c.852_854del	ENSP00000511830.1:p.Met285del
ENST00000695356.1:c.*833_*835del	ENSP00000511831.1:n.*833_*835del
ENST00000695357.1:c.852_854del	ENSP00000511832.1:p.Met285del
ENST00000695358.1:c.852_854del	ENSP00000511833.1:p.Met285del
ENST00000695359.1:c.*509_*511del	ENSP00000511834.1:n.*509_*511del
ENST00000695360.1:c.852_854del	ENSP00000511835.1:p.Met285del
ENST00000695361.1:c.*89-9341_*89-9339del	ENSP00000511836.1:n.*89-9341_*89-9339del
ENST00000695362.1:c.*172_*174del	ENSP00000511837.1:n.*172_*174del
ENST00000695364.1:n.1190_1192del
ENST00000695365.1:n.1142_1144del
ENST00000695366.1:c.852_854del	ENSP00000511838.1:p.Met285del
ENST00000281038.10:c.852_854del MANE Select	ENSP00000281038.5:p.Met285del
ENST00000281038.9:c.852_854del	ENSP00000281038.5:p.Met285del
ENST00000525345.5:c.342_344del
ENST00000528850.5:c.171_173del	ENSP00000432635.1:p.Met58del
ENST00000529880.1:c.595-12641_595-12639del	ENSP00000432240.1:n.595-12641_595-12639del
NM_001243251.1:c.171_173del	NP_001230180.1:p.Met58del
NM_024678.5:c.852_854del	NP_078954.4:p.Met285del
XM_011545253.1:c.852_854del	XP_011543555.1:p.Met285del
XR_950050.1:n.1221_1223del
XR_950051.1:n.1221_1223del
XR_950344.1:n.199+3775_199+3777del
XR_950345.1:n.151+5356_151+5358del
XM_011545253.2:c.852_854del	XP_011543555.1:p.Met285del
XM_017018302.2:c.852_854del	XP_016873791.1:p.Met285del
XM_017018303.1:c.171_173del	XP_016873792.1:p.Met58del
XM_017018304.2:c.171_173del	XP_016873793.1:p.Met58del
XR_001747963.2:n.1206_1208del
XR_001747964.2:n.1206_1208del
XR_001747965.2:n.1206_1208del
XR_001747966.2:n.1206_1208del
XR_001748314.1:n.3035+3775_3035+3777del
NM_024678.6:c.852_854del MANE Select	NP_078954.4:p.Met285del
NM_001243251.2:c.171_173del	NP_001230180.1:p.Met58del