Canonical Allele Identifier: CA1984717758
Gene: NARS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.78478599C= , CM000673.2:g.78478599C= GRCh38
NC_000011.9:g.78189645C= , CM000673.1:g.78189645C= GRCh37
NC_000011.8:g.77867293C= NCBI36
NG_042046.1:g.101266G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525345.6:n.397G=
ENST00000529771.2:c.226G= ENSP00000435298.2:p.Ala76=
ENST00000695114.1:n.3568G=
ENST00000695115.1:c.226G= ENSP00000511705.1:p.Ala76=
ENST00000695116.1:c.142-9286G= ENSP00000511706.1:n.142-9286G=
ENST00000695341.1:c.*577G= ENSP00000511816.1:n.*577G=
ENST00000695342.1:c.226G= ENSP00000511817.1:p.Ala76=
ENST00000695343.1:c.226G= ENSP00000511818.1:p.Ala76=
ENST00000695344.1:c.826G= ENSP00000511819.1:p.Ala276=
ENST00000695345.1:c.226G= ENSP00000511820.1:p.Ala76=
ENST00000695346.1:c.*324G= ENSP00000511821.1:n.*324G=
ENST00000695347.1:c.*379G= ENSP00000511822.1:n.*379G=
ENST00000695348.1:c.226G= ENSP00000511823.1:p.Ala76=
ENST00000695349.1:c.907G= ENSP00000511824.1:p.Ala303=
ENST00000695350.1:c.*78G= ENSP00000511825.1:n.*78G=
ENST00000695351.1:c.823-12586G= ENSP00000511826.1:n.823-12586G=
ENST00000695352.1:c.55G= ENSP00000511827.1:p.Ala19=
ENST00000695353.1:c.-105-12586G= ENSP00000511828.1:n.-105-12586G=
ENST00000695354.1:c.907G= ENSP00000511829.1:p.Ala303=
ENST00000695355.1:c.907G= ENSP00000511830.1:p.Ala303=
ENST00000695356.1:c.*888G= ENSP00000511831.1:n.*888G=
ENST00000695357.1:c.907G= ENSP00000511832.1:p.Ala303=
ENST00000695358.1:c.907G= ENSP00000511833.1:p.Ala303=
ENST00000695359.1:c.*564G= ENSP00000511834.1:n.*564G=
ENST00000695360.1:c.907G= ENSP00000511835.1:p.Ala303=
ENST00000695361.1:c.*89-9286G= ENSP00000511836.1:n.*89-9286G=
ENST00000695362.1:c.*227G= ENSP00000511837.1:n.*227G=
ENST00000695364.1:n.1245G=
ENST00000695365.1:n.1197G=
ENST00000695366.1:c.907G= ENSP00000511838.1:p.Ala303=
ENST00000281038.10:c.907G= MANE Select ENSP00000281038.5:p.Ala303=
ENST00000281038.9:c.907G= ENSP00000281038.5:p.Ala303=
ENST00000525345.5:c.397G=
ENST00000528850.5:c.226G= ENSP00000432635.1:p.Ala76=
ENST00000529880.1:c.595-12586G= ENSP00000432240.1:n.595-12586G=
NM_001243251.1:c.226G= NP_001230180.1:p.Ala76=
NM_024678.5:c.907G= NP_078954.4:p.Ala303=
XM_011545253.1:c.907G= XP_011543555.1:p.Ala303=
XR_950050.1:n.1276G=
XR_950051.1:n.1276G=
XR_950344.1:n.199+3722C=
XR_950345.1:n.151+5303C=
XM_011545253.2:c.907G= XP_011543555.1:p.Ala303=
XM_017018302.2:c.907G= XP_016873791.1:p.Ala303=
XM_017018303.1:c.226G= XP_016873792.1:p.Ala76=
XM_017018304.2:c.226G= XP_016873793.1:p.Ala76=
XR_001747963.2:n.1261G=
XR_001747964.2:n.1261G=
XR_001747965.2:n.1261G=
XR_001747966.2:n.1261G=
XR_001748314.1:n.3035+3722C=
NM_024678.6:c.907G= MANE Select NP_078954.4:p.Ala303=
NM_001243251.2:c.226G= NP_001230180.1:p.Ala76=