Canonical Allele Identifier: CA382177118
Gene: NARS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.78478663C>G , CM000673.2:g.78478663C>G GRCh38
NC_000011.9:g.78189709C>G , CM000673.1:g.78189709C>G GRCh37
NC_000011.8:g.77867357C>G NCBI36
NG_042046.1:g.101202G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000525345.6:n.333G>C
ENST00000529771.2:c.162G>C ENSP00000435298.2:p.Lys54Asn
ENST00000695114.1:n.3504G>C
ENST00000695115.1:c.162G>C ENSP00000511705.1:p.Lys54Asn
ENST00000695116.1:c.142-9350G>C ENSP00000511706.1:n.142-9350G>C
ENST00000695341.1:c.*513G>C ENSP00000511816.1:n.*513G>C
ENST00000695342.1:c.162G>C ENSP00000511817.1:p.Lys54Asn
ENST00000695343.1:c.162G>C ENSP00000511818.1:p.Lys54Asn
ENST00000695344.1:c.762G>C ENSP00000511819.1:p.Lys254Asn
ENST00000695345.1:c.162G>C ENSP00000511820.1:p.Lys54Asn
ENST00000695346.1:c.*260G>C ENSP00000511821.1:n.*260G>C
ENST00000695347.1:c.*315G>C ENSP00000511822.1:n.*315G>C
ENST00000695348.1:c.162G>C ENSP00000511823.1:p.Lys54Asn
ENST00000695349.1:c.843G>C ENSP00000511824.1:p.Lys281Asn
ENST00000695350.1:c.*14G>C ENSP00000511825.1:n.*14G>C
ENST00000695351.1:c.823-12650G>C ENSP00000511826.1:n.823-12650G>C
ENST00000695352.1:c.-10G>C ENSP00000511827.1:n.-10G>C
ENST00000695353.1:c.-105-12650G>C ENSP00000511828.1:n.-105-12650G>C
ENST00000695354.1:c.843G>C ENSP00000511829.1:p.Lys281Asn
ENST00000695355.1:c.843G>C ENSP00000511830.1:p.Lys281Asn
ENST00000695356.1:c.*824G>C ENSP00000511831.1:n.*824G>C
ENST00000695357.1:c.843G>C ENSP00000511832.1:p.Lys281Asn
ENST00000695358.1:c.843G>C ENSP00000511833.1:p.Lys281Asn
ENST00000695359.1:c.*500G>C ENSP00000511834.1:n.*500G>C
ENST00000695360.1:c.843G>C ENSP00000511835.1:p.Lys281Asn
ENST00000695361.1:c.*89-9350G>C ENSP00000511836.1:n.*89-9350G>C
ENST00000695362.1:c.*163G>C ENSP00000511837.1:n.*163G>C
ENST00000695364.1:n.1181G>C
ENST00000695365.1:n.1133G>C
ENST00000695366.1:c.843G>C ENSP00000511838.1:p.Lys281Asn
ENST00000281038.10:c.843G>C MANE Select ENSP00000281038.5:p.Lys281Asn
ENST00000281038.9:c.843G>C ENSP00000281038.5:p.Lys281Asn
ENST00000525345.5:c.333G>C
ENST00000528850.5:c.162G>C ENSP00000432635.1:p.Lys54Asn
ENST00000529880.1:c.595-12650G>C ENSP00000432240.1:n.595-12650G>C
NM_001243251.1:c.162G>C NP_001230180.1:p.Lys54Asn
NM_024678.5:c.843G>C NP_078954.4:p.Lys281Asn
XM_011545253.1:c.843G>C XP_011543555.1:p.Lys281Asn
XR_950050.1:n.1212G>C
XR_950051.1:n.1212G>C
XR_950344.1:n.199+3786C>G
XR_950345.1:n.151+5367C>G
XM_011545253.2:c.843G>C XP_011543555.1:p.Lys281Asn
XM_017018302.2:c.843G>C XP_016873791.1:p.Lys281Asn
XM_017018303.1:c.162G>C XP_016873792.1:p.Lys54Asn
XM_017018304.2:c.162G>C XP_016873793.1:p.Lys54Asn
XR_001747963.2:n.1197G>C
XR_001747964.2:n.1197G>C
XR_001747965.2:n.1197G>C
XR_001747966.2:n.1197G>C
XR_001748314.1:n.3035+3786C>G
NM_024678.6:c.843G>C MANE Select NP_078954.4:p.Lys281Asn
NM_001243251.2:c.162G>C NP_001230180.1:p.Lys54Asn