Canonical Allele Identifier: CA1525232594

Gene: NSUN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.6619980_6619984delinsGCTAT , CM000667.2:g.6619980_6619984delinsGCTAT	GRCh38
NC_000005.9:g.6620093_6620097delinsGCTAT , CM000667.1:g.6620093_6620097delinsGCTAT	GRCh37
NC_000005.8:g.6673093_6673097delinsGCTAT	NCBI36
NG_028215.1:g.18377_18381delinsATAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264670.11:c.815+122_815+126delinsATAGC MANE Select	ENSP00000264670.6:n.815+122_815+126delinsATAGC
ENST00000264670.10:c.815+122_815+126delinsATAGC	ENSP00000264670.6:n.815+122_815+126delinsATAGC
ENST00000504374.5:c.*121+122_*121+126delinsATAGC	ENSP00000421783.1:n.*121+122_*121+126delinsATAGC
ENST00000505892.5:n.1384+122_1384+126delinsATAGC
ENST00000506139.5:c.710+122_710+126delinsATAGC	ENSP00000420957.1:n.710+122_710+126delinsATAGC
NM_001193455.1:c.710+122_710+126delinsATAGC	NP_001180384.1:n.710+122_710+126delinsATAGC
NM_017755.5:c.815+122_815+126delinsATAGC	NP_060225.4:n.815+122_815+126delinsATAGC
NR_037947.1:n.1111+122_1111+126delinsATAGC
NM_017755.6:c.815+122_815+126delinsATAGC MANE Select	NP_060225.4:n.815+122_815+126delinsATAGC
NM_001193455.2:c.710+122_710+126delinsATAGC	NP_001180384.1:n.710+122_710+126delinsATAGC
NR_037947.2:n.795+122_795+126delinsATAGC