Canonical Allele Identifier: CA1525237851

Gene: NSUN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.6611077C= , CM000667.2:g.6611077C=	GRCh38
NC_000005.9:g.6611190C= , CM000667.1:g.6611190C=	GRCh37
NC_000005.8:g.6664190C=	NCBI36
NG_028215.1:g.27284G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264670.11:c.1104G= MANE Select	ENSP00000264670.6:p.Thr368=
ENST00000264670.10:c.1104G=	ENSP00000264670.6:p.Thr368=
ENST00000504374.5:c.*410G=	ENSP00000421783.1:n.*410G=
ENST00000505892.5:n.1673G=
ENST00000506139.5:c.999G=	ENSP00000420957.1:p.Thr333=
NM_001193455.1:c.999G=	NP_001180384.1:p.Thr333=
NM_017755.5:c.1104G=	NP_060225.4:p.Thr368=
NR_037947.1:n.1400G=
NM_017755.6:c.1104G= MANE Select	NP_060225.4:p.Thr368=
NM_001193455.2:c.999G=	NP_001180384.1:p.Thr333=
NR_037947.2:n.1084G=