Canonical Allele Identifier: CA1525242326

Gene: NSUN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.6629817G= , CM000667.2:g.6629817G=	GRCh38
NC_000005.9:g.6629930G= , CM000667.1:g.6629930G=	GRCh37
NC_000005.8:g.6682930G=	NCBI36
NG_028215.1:g.8544C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264670.11:c.359+2056C= MANE Select	ENSP00000264670.6:n.359+2056C=
ENST00000264670.10:c.359+2056C=	ENSP00000264670.6:n.359+2056C=
ENST00000504374.5:c.359+2056C=	ENSP00000421783.1:n.359+2056C=
ENST00000506139.5:c.254+2782C=	ENSP00000420957.1:n.254+2782C=
NM_001193455.1:c.254+2782C=	NP_001180384.1:n.254+2782C=
NM_017755.5:c.359+2056C=	NP_060225.4:n.359+2056C=
NR_037947.1:n.740+2056C=
NM_017755.6:c.359+2056C= MANE Select	NP_060225.4:n.359+2056C=
NM_001193455.2:c.254+2782C=	NP_001180384.1:n.254+2782C=
NR_037947.2:n.424+2056C=