Canonical Allele Identifier: CA1525232815

Gene: NSUN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.6620159G= , CM000667.2:g.6620159G=	GRCh38
NC_000005.9:g.6620272G= , CM000667.1:g.6620272G=	GRCh37
NC_000005.8:g.6673272G=	NCBI36
NG_028215.1:g.18202C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264670.11:c.762C= MANE Select	ENSP00000264670.6:p.Asp254=
ENST00000264670.10:c.762C=	ENSP00000264670.6:p.Asp254=
ENST00000504374.5:c.*68C=	ENSP00000421783.1:n.*68C=
ENST00000505264.1:n.429C=
ENST00000505892.5:n.1331C=
ENST00000506139.5:c.657C=	ENSP00000420957.1:p.Asp219=
NM_001193455.1:c.657C=	NP_001180384.1:p.Asp219=
NM_017755.5:c.762C=	NP_060225.4:p.Asp254=
NR_037947.1:n.1058C=
NM_017755.6:c.762C= MANE Select	NP_060225.4:p.Asp254=
NM_001193455.2:c.657C=	NP_001180384.1:p.Asp219=
NR_037947.2:n.742C=