Canonical Allele Identifier: CA1525232451

Gene: NSUN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.6619898_6619900delinsCCT , CM000667.2:g.6619898_6619900delinsCCT	GRCh38
NC_000005.9:g.6620011_6620013delinsCCT , CM000667.1:g.6620011_6620013delinsCCT	GRCh37
NC_000005.8:g.6673011_6673013delinsCCT	NCBI36
NG_028215.1:g.18461_18463delinsAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264670.11:c.815+206_815+208delinsAGG MANE Select	ENSP00000264670.6:n.815+206_815+208delinsAGG
ENST00000264670.10:c.815+206_815+208delinsAGG	ENSP00000264670.6:n.815+206_815+208delinsAGG
ENST00000504374.5:c.*121+206_*121+208delinsAGG	ENSP00000421783.1:n.*121+206_*121+208delinsAGG
ENST00000505892.5:n.1384+206_1384+208delinsAGG
ENST00000506139.5:c.710+206_710+208delinsAGG	ENSP00000420957.1:n.710+206_710+208delinsAGG
NM_001193455.1:c.710+206_710+208delinsAGG	NP_001180384.1:n.710+206_710+208delinsAGG
NM_017755.5:c.815+206_815+208delinsAGG	NP_060225.4:n.815+206_815+208delinsAGG
NR_037947.1:n.1111+206_1111+208delinsAGG
NM_017755.6:c.815+206_815+208delinsAGG MANE Select	NP_060225.4:n.815+206_815+208delinsAGG
NM_001193455.2:c.710+206_710+208delinsAGG	NP_001180384.1:n.710+206_710+208delinsAGG
NR_037947.2:n.795+206_795+208delinsAGG