Canonical Allele Identifier: CA1525232863

Gene: NSUN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.6620181G= , CM000667.2:g.6620181G=	GRCh38
NC_000005.9:g.6620294G= , CM000667.1:g.6620294G=	GRCh37
NC_000005.8:g.6673294G=	NCBI36
NG_028215.1:g.18180C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264670.11:c.740C= MANE Select	ENSP00000264670.6:p.Pro247=
ENST00000264670.10:c.740C=	ENSP00000264670.6:p.Pro247=
ENST00000504374.5:c.*46C=	ENSP00000421783.1:n.*46C=
ENST00000505264.1:n.407C=
ENST00000505892.5:n.1309C=
ENST00000506139.5:c.635C=	ENSP00000420957.1:p.Pro212=
NM_001193455.1:c.635C=	NP_001180384.1:p.Pro212=
NM_017755.5:c.740C=	NP_060225.4:p.Pro247=
NR_037947.1:n.1036C=
NM_017755.6:c.740C= MANE Select	NP_060225.4:p.Pro247=
NM_001193455.2:c.635C=	NP_001180384.1:p.Pro212=
NR_037947.2:n.720C=