Canonical Allele Identifier: CA645540879

Gene: NSUN2

Linked Data

• COSMIC: COSM6104421

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.6620157_6620158delinsAA , CM000667.2:g.6620157_6620158delinsAA	GRCh38
NC_000005.9:g.6620270_6620271delinsAA , CM000667.1:g.6620270_6620271delinsAA	GRCh37
NC_000005.8:g.6673270_6673271delinsAA	NCBI36
NG_028215.1:g.18203_18204delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264670.11:c.763_764delinsTT MANE Select	ENSP00000264670.6:p.Gly255Phe
ENST00000264670.10:c.763_764delinsTT	ENSP00000264670.6:p.Gly255Phe
ENST00000504374.5:c.*69_*70delinsTT	ENSP00000421783.1:n.*69_*70delinsTT
ENST00000505264.1:n.430_431delinsTT
ENST00000505892.5:n.1332_1333delinsTT
ENST00000506139.5:c.658_659delinsTT	ENSP00000420957.1:p.Gly220Phe
NM_001193455.1:c.658_659delinsTT	NP_001180384.1:p.Gly220Phe
NM_017755.5:c.763_764delinsTT	NP_060225.4:p.Gly255Phe
NR_037947.1:n.1059_1060delinsTT
NM_017755.6:c.763_764delinsTT MANE Select	NP_060225.4:p.Gly255Phe
NM_001193455.2:c.658_659delinsTT	NP_001180384.1:p.Gly220Phe
NR_037947.2:n.743_744delinsTT