Canonical Allele Identifier: CA1525232857

Gene: NSUN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.6620176G= , CM000667.2:g.6620176G=	GRCh38
NC_000005.9:g.6620289G= , CM000667.1:g.6620289G=	GRCh37
NC_000005.8:g.6673289G=	NCBI36
NG_028215.1:g.18185C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264670.11:c.745C= MANE Select	ENSP00000264670.6:p.Leu249=
ENST00000264670.10:c.745C=	ENSP00000264670.6:p.Leu249=
ENST00000504374.5:c.*51C=	ENSP00000421783.1:n.*51C=
ENST00000505264.1:n.412C=
ENST00000505892.5:n.1314C=
ENST00000506139.5:c.640C=	ENSP00000420957.1:p.Leu214=
NM_001193455.1:c.640C=	NP_001180384.1:p.Leu214=
NM_017755.5:c.745C=	NP_060225.4:p.Leu249=
NR_037947.1:n.1041C=
NM_017755.6:c.745C= MANE Select	NP_060225.4:p.Leu249=
NM_001193455.2:c.640C=	NP_001180384.1:p.Leu214=
NR_037947.2:n.725C=