Canonical Allele Identifier: CA355990843

Gene: NSD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1955849G>A , CM000666.2:g.1955849G>A	GRCh38
NC_000004.11:g.1957576G>A , CM000666.1:g.1957576G>A	GRCh37
NC_000004.10:g.1927374G>A	NCBI36
NG_009269.1:g.89454G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508803.6:c.2675G>A MANE Select	ENSP00000423972.1:p.Arg892Lys
ENST00000677559.1:c.*441G>A	ENSP00000504406.1:n.*441G>A
ENST00000312087.10:c.*958G>A	ENSP00000308780.6:n.*958G>A
ENST00000353275.9:c.*825G>A	ENSP00000329167.5:n.*825G>A
ENST00000382888.3:c.719G>A	ENSP00000372344.3:p.Arg240Lys
ENST00000382891.9:c.2675G>A	ENSP00000372347.5:p.Arg892Lys
ENST00000382892.6:c.2675G>A	ENSP00000372348.2:p.Arg892Lys
ENST00000382895.7:c.2675G>A	ENSP00000372351.3:p.Arg892Lys
ENST00000482415.6:n.1292G>A
ENST00000503207.1:n.608G>A
ENST00000505643.5:n.814G>A
ENST00000507094.1:n.271G>A
ENST00000508803.5:c.2675G>A	ENSP00000423972.1:p.Arg892Lys
ENST00000514329.5:c.645G>A
NM_001042424.2:c.2675G>A	NP_001035889.1:p.Arg892Lys
NM_133330.2:c.2675G>A	NP_579877.1:p.Arg892Lys
NM_133331.2:c.2675G>A	NP_579878.1:p.Arg892Lys
NM_133335.3:c.2675G>A	NP_579890.1:p.Arg892Lys
XM_005248001.3:c.2675G>A	XP_005248058.1:p.Arg892Lys
XM_005248002.1:c.2468G>A	XP_005248059.1:p.Arg823Lys
XM_006713915.2:c.332G>A	XP_006713978.1:p.Arg111Lys
XM_011513557.1:c.2675G>A	XP_011511859.1:p.Arg892Lys
XM_011513558.1:c.2675G>A	XP_011511860.1:p.Arg892Lys
XM_011513559.1:c.719G>A	XP_011511861.1:p.Arg240Lys
XM_011513560.1:c.332G>A	XP_011511862.1:p.Arg111Lys
XM_005248001.4:c.2675G>A	XP_005248058.1:p.Arg892Lys
XM_005248002.3:c.2468G>A	XP_005248059.1:p.Arg823Lys
XM_011513557.2:c.2675G>A	XP_011511859.1:p.Arg892Lys
XM_011513560.2:c.332G>A	XP_011511862.1:p.Arg111Lys
XM_017008587.1:c.332G>A	XP_016864076.1:p.Arg111Lys
XM_017008588.1:c.332G>A	XP_016864077.1:p.Arg111Lys
NM_001042424.3:c.2675G>A MANE Select	NP_001035889.1:p.Arg892Lys
NM_133330.3:c.2675G>A	NP_579877.1:p.Arg892Lys
NM_133331.3:c.2675G>A	NP_579878.1:p.Arg892Lys
NM_133335.4:c.2675G>A	NP_579890.1:p.Arg892Lys