Canonical Allele Identifier: CA1525232629

Gene: NSUN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.6620008T= , CM000667.2:g.6620008T=	GRCh38
NC_000005.9:g.6620121T= , CM000667.1:g.6620121T=	GRCh37
NC_000005.8:g.6673121T=	NCBI36
NG_028215.1:g.18353A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264670.11:c.815+98A= MANE Select	ENSP00000264670.6:n.815+98A=
ENST00000264670.10:c.815+98A=	ENSP00000264670.6:n.815+98A=
ENST00000504374.5:c.*121+98A=	ENSP00000421783.1:n.*121+98A=
ENST00000505892.5:n.1384+98A=
ENST00000506139.5:c.710+98A=	ENSP00000420957.1:n.710+98A=
NM_001193455.1:c.710+98A=	NP_001180384.1:n.710+98A=
NM_017755.5:c.815+98A=	NP_060225.4:n.815+98A=
NR_037947.1:n.1111+98A=
NM_017755.6:c.815+98A= MANE Select	NP_060225.4:n.815+98A=
NM_001193455.2:c.710+98A=	NP_001180384.1:n.710+98A=
NR_037947.2:n.795+98A=