Canonical Allele Identifier: CA1525232408

Gene: NSUN2

Linked Data

• dbSNP Id: rs1737364116

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.6619869_6619870del , CM000667.2:g.6619869_6619870del	GRCh38
NC_000005.9:g.6619982_6619983del , CM000667.1:g.6619982_6619983del	GRCh37
NC_000005.8:g.6672982_6672983del	NCBI36
NG_028215.1:g.18492_18493del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264670.11:c.815+237_815+238del MANE Select	ENSP00000264670.6:n.815+237_815+238del
ENST00000264670.10:c.815+237_815+238del	ENSP00000264670.6:n.815+237_815+238del
ENST00000504374.5:c.*121+237_*121+238del	ENSP00000421783.1:n.*121+237_*121+238del
ENST00000505892.5:n.1384+237_1384+238del
ENST00000506139.5:c.710+237_710+238del	ENSP00000420957.1:n.710+237_710+238del
NM_001193455.1:c.710+237_710+238del	NP_001180384.1:n.710+237_710+238del
NM_017755.5:c.815+237_815+238del	NP_060225.4:n.815+237_815+238del
NR_037947.1:n.1111+237_1111+238del
NM_017755.6:c.815+237_815+238del MANE Select	NP_060225.4:n.815+237_815+238del
NM_001193455.2:c.710+237_710+238del	NP_001180384.1:n.710+237_710+238del
NR_037947.2:n.795+237_795+238del