Canonical Allele Identifier: CA355997711

Gene: NSD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1961132A>G , CM000666.2:g.1961132A>G	GRCh38
NC_000004.11:g.1962859A>G , CM000666.1:g.1962859A>G	GRCh37
NC_000004.10:g.1932657A>G	NCBI36
NG_009269.1:g.94737A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508803.6:c.3353A>G MANE Select	ENSP00000423972.1:p.Tyr1118Cys
ENST00000677559.1:c.*1119A>G	ENSP00000504406.1:n.*1119A>G
ENST00000679039.1:n.543A>G
ENST00000312087.10:c.*1636A>G	ENSP00000308780.6:n.*1636A>G
ENST00000353275.9:c.*1503A>G	ENSP00000329167.5:n.*1503A>G
ENST00000382888.3:c.1397A>G	ENSP00000372344.3:p.Tyr466Cys
ENST00000382891.9:c.3353A>G	ENSP00000372347.5:p.Tyr1118Cys
ENST00000382892.6:c.3353A>G	ENSP00000372348.2:p.Tyr1118Cys
ENST00000382895.7:c.3353A>G	ENSP00000372351.3:p.Tyr1118Cys
ENST00000482415.6:n.1970A>G
ENST00000508803.5:c.3353A>G	ENSP00000423972.1:p.Tyr1118Cys
NM_001042424.2:c.3353A>G	NP_001035889.1:p.Tyr1118Cys
NM_133330.2:c.3353A>G	NP_579877.1:p.Tyr1118Cys
NM_133331.2:c.3353A>G	NP_579878.1:p.Tyr1118Cys
NM_133335.3:c.3353A>G	NP_579890.1:p.Tyr1118Cys
XM_005248001.3:c.3353A>G	XP_005248058.1:p.Tyr1118Cys
XM_005248002.1:c.3146A>G	XP_005248059.1:p.Tyr1049Cys
XM_006713915.2:c.1010A>G	XP_006713978.1:p.Tyr337Cys
XM_011513557.1:c.3353A>G	XP_011511859.1:p.Tyr1118Cys
XM_011513558.1:c.3353A>G	XP_011511860.1:p.Tyr1118Cys
XM_011513559.1:c.1397A>G	XP_011511861.1:p.Tyr466Cys
XM_011513560.1:c.1010A>G	XP_011511862.1:p.Tyr337Cys
XM_005248001.4:c.3353A>G	XP_005248058.1:p.Tyr1118Cys
XM_005248002.3:c.3146A>G	XP_005248059.1:p.Tyr1049Cys
XM_011513557.2:c.3353A>G	XP_011511859.1:p.Tyr1118Cys
XM_011513560.2:c.1010A>G	XP_011511862.1:p.Tyr337Cys
XM_017008587.1:c.1010A>G	XP_016864076.1:p.Tyr337Cys
XM_017008588.1:c.1010A>G	XP_016864077.1:p.Tyr337Cys
NM_001042424.3:c.3353A>G MANE Select	NP_001035889.1:p.Tyr1118Cys
NM_133330.3:c.3353A>G	NP_579877.1:p.Tyr1118Cys
NM_133331.3:c.3353A>G	NP_579878.1:p.Tyr1118Cys
NM_133335.4:c.3353A>G	NP_579890.1:p.Tyr1118Cys