Canonical Allele Identifier: CA382177067
Gene: NARS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.78478636T>G , CM000673.2:g.78478636T>G GRCh38
NC_000011.9:g.78189682T>G , CM000673.1:g.78189682T>G GRCh37
NC_000011.8:g.77867330T>G NCBI36
NG_042046.1:g.101229A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000525345.6:n.360A>C
ENST00000529771.2:c.189A>C ENSP00000435298.2:p.Lys63Asn
ENST00000695114.1:n.3531A>C
ENST00000695115.1:c.189A>C ENSP00000511705.1:p.Lys63Asn
ENST00000695116.1:c.142-9323A>C ENSP00000511706.1:n.142-9323A>C
ENST00000695341.1:c.*540A>C ENSP00000511816.1:n.*540A>C
ENST00000695342.1:c.189A>C ENSP00000511817.1:p.Lys63Asn
ENST00000695343.1:c.189A>C ENSP00000511818.1:p.Lys63Asn
ENST00000695344.1:c.789A>C ENSP00000511819.1:p.Lys263Asn
ENST00000695345.1:c.189A>C ENSP00000511820.1:p.Lys63Asn
ENST00000695346.1:c.*287A>C ENSP00000511821.1:n.*287A>C
ENST00000695347.1:c.*342A>C ENSP00000511822.1:n.*342A>C
ENST00000695348.1:c.189A>C ENSP00000511823.1:p.Lys63Asn
ENST00000695349.1:c.870A>C ENSP00000511824.1:p.Lys290Asn
ENST00000695350.1:c.*41A>C ENSP00000511825.1:n.*41A>C
ENST00000695351.1:c.823-12623A>C ENSP00000511826.1:n.823-12623A>C
ENST00000695352.1:c.18A>C ENSP00000511827.1:p.Lys6Asn
ENST00000695353.1:c.-105-12623A>C ENSP00000511828.1:n.-105-12623A>C
ENST00000695354.1:c.870A>C ENSP00000511829.1:p.Lys290Asn
ENST00000695355.1:c.870A>C ENSP00000511830.1:p.Lys290Asn
ENST00000695356.1:c.*851A>C ENSP00000511831.1:n.*851A>C
ENST00000695357.1:c.870A>C ENSP00000511832.1:p.Lys290Asn
ENST00000695358.1:c.870A>C ENSP00000511833.1:p.Lys290Asn
ENST00000695359.1:c.*527A>C ENSP00000511834.1:n.*527A>C
ENST00000695360.1:c.870A>C ENSP00000511835.1:p.Lys290Asn
ENST00000695361.1:c.*89-9323A>C ENSP00000511836.1:n.*89-9323A>C
ENST00000695362.1:c.*190A>C ENSP00000511837.1:n.*190A>C
ENST00000695364.1:n.1208A>C
ENST00000695365.1:n.1160A>C
ENST00000695366.1:c.870A>C ENSP00000511838.1:p.Lys290Asn
ENST00000281038.10:c.870A>C MANE Select ENSP00000281038.5:p.Lys290Asn
ENST00000281038.9:c.870A>C ENSP00000281038.5:p.Lys290Asn
ENST00000525345.5:c.360A>C
ENST00000528850.5:c.189A>C ENSP00000432635.1:p.Lys63Asn
ENST00000529880.1:c.595-12623A>C ENSP00000432240.1:n.595-12623A>C
NM_001243251.1:c.189A>C NP_001230180.1:p.Lys63Asn
NM_024678.5:c.870A>C NP_078954.4:p.Lys290Asn
XM_011545253.1:c.870A>C XP_011543555.1:p.Lys290Asn
XR_950050.1:n.1239A>C
XR_950051.1:n.1239A>C
XR_950344.1:n.199+3759T>G
XR_950345.1:n.151+5340T>G
XM_011545253.2:c.870A>C XP_011543555.1:p.Lys290Asn
XM_017018302.2:c.870A>C XP_016873791.1:p.Lys290Asn
XM_017018303.1:c.189A>C XP_016873792.1:p.Lys63Asn
XM_017018304.2:c.189A>C XP_016873793.1:p.Lys63Asn
XR_001747963.2:n.1224A>C
XR_001747964.2:n.1224A>C
XR_001747965.2:n.1224A>C
XR_001747966.2:n.1224A>C
XR_001748314.1:n.3035+3759T>G
NM_024678.6:c.870A>C MANE Select NP_078954.4:p.Lys290Asn
NM_001243251.2:c.189A>C NP_001230180.1:p.Lys63Asn