Canonical Allele Identifier: CA1525232849

Gene: NSUN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.6620175A= , CM000667.2:g.6620175A=	GRCh38
NC_000005.9:g.6620288A= , CM000667.1:g.6620288A=	GRCh37
NC_000005.8:g.6673288A=	NCBI36
NG_028215.1:g.18186T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264670.11:c.746T= MANE Select	ENSP00000264670.6:p.Leu249=
ENST00000264670.10:c.746T=	ENSP00000264670.6:p.Leu249=
ENST00000504374.5:c.*52T=	ENSP00000421783.1:n.*52T=
ENST00000505264.1:n.413T=
ENST00000505892.5:n.1315T=
ENST00000506139.5:c.641T=	ENSP00000420957.1:p.Leu214=
NM_001193455.1:c.641T=	NP_001180384.1:p.Leu214=
NM_017755.5:c.746T=	NP_060225.4:p.Leu249=
NR_037947.1:n.1042T=
NM_017755.6:c.746T= MANE Select	NP_060225.4:p.Leu249=
NM_001193455.2:c.641T=	NP_001180384.1:p.Leu214=
NR_037947.2:n.726T=