Canonical Allele Identifier: CA1525232692
Gene: NSUN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.6620060_6620066delinsTGATTTC , CM000667.2:g.6620060_6620066delinsTGATTTC GRCh38
NC_000005.9:g.6620173_6620179delinsTGATTTC , CM000667.1:g.6620173_6620179delinsTGATTTC GRCh37
NC_000005.8:g.6673173_6673179delinsTGATTTC NCBI36
NG_028215.1:g.18295_18301delinsGAAATCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000264670.11:c.815+40_815+46delinsGAAATCA MANE Select ENSP00000264670.6:n.815+40_815+46delinsGAAATCA
ENST00000264670.10:c.815+40_815+46delinsGAAATCA ENSP00000264670.6:n.815+40_815+46delinsGAAATCA
ENST00000504374.5:c.*121+40_*121+46delinsGAAATCA ENSP00000421783.1:n.*121+40_*121+46delinsGAAATCA
ENST00000505892.5:n.1384+40_1384+46delinsGAAATCA
ENST00000506139.5:c.710+40_710+46delinsGAAATCA ENSP00000420957.1:n.710+40_710+46delinsGAAATCA
NM_001193455.1:c.710+40_710+46delinsGAAATCA NP_001180384.1:n.710+40_710+46delinsGAAATCA
NM_017755.5:c.815+40_815+46delinsGAAATCA NP_060225.4:n.815+40_815+46delinsGAAATCA
NR_037947.1:n.1111+40_1111+46delinsGAAATCA
NM_017755.6:c.815+40_815+46delinsGAAATCA MANE Select NP_060225.4:n.815+40_815+46delinsGAAATCA
NM_001193455.2:c.710+40_710+46delinsGAAATCA NP_001180384.1:n.710+40_710+46delinsGAAATCA
NR_037947.2:n.795+40_795+46delinsGAAATCA