Canonical Allele Identifier: CA2615327783
Gene: NARS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.78478582del , CM000673.2:g.78478582del GRCh38
NC_000011.9:g.78189628del , CM000673.1:g.78189628del GRCh37
NC_000011.8:g.77867276del NCBI36
NG_042046.1:g.101284del

Transcript Alleles

HGVS Amino-acid Change
ENST00000525345.6:n.411+4del
ENST00000529771.2:c.240+4del ENSP00000435298.2:n.240+4del
ENST00000695114.1:n.3582+4del
ENST00000695115.1:c.240+4del ENSP00000511705.1:n.240+4del
ENST00000695116.1:c.142-9268del ENSP00000511706.1:n.142-9268del
ENST00000695341.1:c.*591+4del ENSP00000511816.1:n.*591+4del
ENST00000695342.1:c.240+4del ENSP00000511817.1:n.240+4del
ENST00000695343.1:c.240+4del ENSP00000511818.1:n.240+4del
ENST00000695344.1:c.840+4del ENSP00000511819.1:n.840+4del
ENST00000695345.1:c.240+4del ENSP00000511820.1:n.240+4del
ENST00000695346.1:c.*338+4del ENSP00000511821.1:n.*338+4del
ENST00000695347.1:c.*393+4del ENSP00000511822.1:n.*393+4del
ENST00000695348.1:c.240+4del ENSP00000511823.1:n.240+4del
ENST00000695349.1:c.921+4del ENSP00000511824.1:n.921+4del
ENST00000695350.1:c.*92+4del ENSP00000511825.1:n.*92+4del
ENST00000695351.1:c.823-12568del ENSP00000511826.1:n.823-12568del
ENST00000695352.1:c.69+4del ENSP00000511827.1:n.69+4del
ENST00000695353.1:c.-105-12568del ENSP00000511828.1:n.-105-12568del
ENST00000695354.1:c.921+4del ENSP00000511829.1:n.921+4del
ENST00000695355.1:c.921+4del ENSP00000511830.1:n.921+4del
ENST00000695356.1:c.*902+4del ENSP00000511831.1:n.*902+4del
ENST00000695357.1:c.921+4del ENSP00000511832.1:n.921+4del
ENST00000695358.1:c.921+4del ENSP00000511833.1:n.921+4del
ENST00000695359.1:c.*578+4del ENSP00000511834.1:n.*578+4del
ENST00000695360.1:c.921+4del ENSP00000511835.1:n.921+4del
ENST00000695361.1:c.*89-9268del ENSP00000511836.1:n.*89-9268del
ENST00000695362.1:c.*241+4del ENSP00000511837.1:n.*241+4del
ENST00000695364.1:n.1259+4del
ENST00000695365.1:n.1215del
ENST00000695366.1:c.921+4del ENSP00000511838.1:n.921+4del
ENST00000281038.10:c.921+4del MANE Select ENSP00000281038.5:n.921+4del
ENST00000281038.9:c.921+4del ENSP00000281038.5:n.921+4del
ENST00000525345.5:c.411+4del
ENST00000528850.5:c.240+4del ENSP00000432635.1:n.240+4del
ENST00000529880.1:c.595-12568del ENSP00000432240.1:n.595-12568del
NM_001243251.1:c.240+4del NP_001230180.1:n.240+4del
NM_024678.5:c.921+4del NP_078954.4:n.921+4del
XM_011545253.1:c.921+4del XP_011543555.1:n.921+4del
XR_950050.1:n.1290+4del
XR_950051.1:n.1290+4del
XR_950344.1:n.199+3705del
XR_950345.1:n.151+5286del
XM_011545253.2:c.921+4del XP_011543555.1:n.921+4del
XM_017018302.2:c.921+4del XP_016873791.1:n.921+4del
XM_017018303.1:c.240+4del XP_016873792.1:n.240+4del
XM_017018304.2:c.240+4del XP_016873793.1:n.240+4del
XR_001747963.2:n.1275+4del
XR_001747964.2:n.1275+4del
XR_001747965.2:n.1275+4del
XR_001747966.2:n.1275+4del
XR_001748314.1:n.3035+3705del
NM_024678.6:c.921+4del MANE Select NP_078954.4:n.921+4del
NM_001243251.2:c.240+4del NP_001230180.1:n.240+4del