Canonical Allele Identifier: CA1525232545

Gene: NSUN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.6619945_6619946delinsCG , CM000667.2:g.6619945_6619946delinsCG	GRCh38
NC_000005.9:g.6620058_6620059delinsCG , CM000667.1:g.6620058_6620059delinsCG	GRCh37
NC_000005.8:g.6673058_6673059delinsCG	NCBI36
NG_028215.1:g.18415_18416delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264670.11:c.815+160_815+161delinsCG MANE Select	ENSP00000264670.6:n.815+160_815+161delinsCG
ENST00000264670.10:c.815+160_815+161delinsCG	ENSP00000264670.6:n.815+160_815+161delinsCG
ENST00000504374.5:c.*121+160_*121+161delinsCG	ENSP00000421783.1:n.*121+160_*121+161delinsCG
ENST00000505892.5:n.1384+160_1384+161delinsCG
ENST00000506139.5:c.710+160_710+161delinsCG	ENSP00000420957.1:n.710+160_710+161delinsCG
NM_001193455.1:c.710+160_710+161delinsCG	NP_001180384.1:n.710+160_710+161delinsCG
NM_017755.5:c.815+160_815+161delinsCG	NP_060225.4:n.815+160_815+161delinsCG
NR_037947.1:n.1111+160_1111+161delinsCG
NM_017755.6:c.815+160_815+161delinsCG MANE Select	NP_060225.4:n.815+160_815+161delinsCG
NM_001193455.2:c.710+160_710+161delinsCG	NP_001180384.1:n.710+160_710+161delinsCG
NR_037947.2:n.795+160_795+161delinsCG