Canonical Allele Identifier: CA1525232405

Gene: NSUN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.6619867_6619869delinsCTT , CM000667.2:g.6619867_6619869delinsCTT	GRCh38
NC_000005.9:g.6619980_6619982delinsCTT , CM000667.1:g.6619980_6619982delinsCTT	GRCh37
NC_000005.8:g.6672980_6672982delinsCTT	NCBI36
NG_028215.1:g.18492_18494delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264670.11:c.815+237_815+239delinsAAG MANE Select	ENSP00000264670.6:n.815+237_815+239delinsAAG
ENST00000264670.10:c.815+237_815+239delinsAAG	ENSP00000264670.6:n.815+237_815+239delinsAAG
ENST00000504374.5:c.*121+237_*121+239delinsAAG	ENSP00000421783.1:n.*121+237_*121+239delinsAAG
ENST00000505892.5:n.1384+237_1384+239delinsAAG
ENST00000506139.5:c.710+237_710+239delinsAAG	ENSP00000420957.1:n.710+237_710+239delinsAAG
NM_001193455.1:c.710+237_710+239delinsAAG	NP_001180384.1:n.710+237_710+239delinsAAG
NM_017755.5:c.815+237_815+239delinsAAG	NP_060225.4:n.815+237_815+239delinsAAG
NR_037947.1:n.1111+237_1111+239delinsAAG
NM_017755.6:c.815+237_815+239delinsAAG MANE Select	NP_060225.4:n.815+237_815+239delinsAAG
NM_001193455.2:c.710+237_710+239delinsAAG	NP_001180384.1:n.710+237_710+239delinsAAG
NR_037947.2:n.795+237_795+239delinsAAG