Canonical Allele Identifier: CA1433597914

Gene: NSD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1980828_1980835delinsCTCTAACT , CM000666.2:g.1980828_1980835delinsCTCTAACT	GRCh38
NC_000004.11:g.1982555_1982562delinsCTCTAACT , CM000666.1:g.1982555_1982562delinsCTCTAACT	GRCh37
NC_000004.10:g.1952353_1952360delinsCTCTAACT	NCBI36
NG_009232.1:g.33398_33405delinsAGTTAGAG
NG_009269.1:g.114433_114440delinsCTCTAACT

Transcript Alleles

HGVS	Amino-acid change
ENST00000508803.6:c.*1919_*1926delinsCTCTAACT MANE Select	ENSP00000423972.1:n.*1919_*1926delinsCTCTAACT
ENST00000677559.1:c.*3783_*3790delinsCTCTAACT	ENSP00000504406.1:n.*3783_*3790delinsCTCTAACT
ENST00000677895.1:c.*1919_*1926delinsCTCTAACT	ENSP00000503076.1:n.*1919_*1926delinsCTCTAACT
ENST00000679039.1:n.3207_3214delinsCTCTAACT
ENST00000312087.10:c.*4300_*4307delinsCTCTAACT	ENSP00000308780.6:n.*4300_*4307delinsCTCTAACT
ENST00000353275.9:c.*4167_*4174delinsCTCTAACT	ENSP00000329167.5:n.*4167_*4174delinsCTCTAACT
ENST00000382891.9:c.*1919_*1926delinsCTCTAACT	ENSP00000372347.5:n.*1919_*1926delinsCTCTAACT
ENST00000382892.6:c.*1919_*1926delinsCTCTAACT	ENSP00000372348.2:n.*1919_*1926delinsCTCTAACT
ENST00000382895.7:c.*1919_*1926delinsCTCTAACT	ENSP00000372351.3:n.*1919_*1926delinsCTCTAACT
NM_001042424.2:c.*1919_*1926delinsCTCTAACT	NP_001035889.1:n.*1919_*1926delinsCTCTAACT
NM_133330.2:c.*1919_*1926delinsCTCTAACT	NP_579877.1:n.*1919_*1926delinsCTCTAACT
NM_133331.2:c.*1919_*1926delinsCTCTAACT	NP_579878.1:n.*1919_*1926delinsCTCTAACT
NM_133335.3:c.*1919_*1926delinsCTCTAACT	NP_579890.1:n.*1919_*1926delinsCTCTAACT
XM_005248001.3:c.*1919_*1926delinsCTCTAACT	XP_005248058.1:n.*1919_*1926delinsCTCTAACT
XM_005248002.1:c.*1919_*1926delinsCTCTAACT	XP_005248059.1:n.*1919_*1926delinsCTCTAACT
XM_006713915.2:c.*1919_*1926delinsCTCTAACT	XP_006713978.1:n.*1919_*1926delinsCTCTAACT
XM_011513557.1:c.*1919_*1926delinsCTCTAACT	XP_011511859.1:n.*1919_*1926delinsCTCTAACT
XM_011513558.1:c.*1919_*1926delinsCTCTAACT	XP_011511860.1:n.*1919_*1926delinsCTCTAACT
XM_011513559.1:c.*1919_*1926delinsCTCTAACT	XP_011511861.1:n.*1919_*1926delinsCTCTAACT
XM_011513560.1:c.*1919_*1926delinsCTCTAACT	XP_011511862.1:n.*1919_*1926delinsCTCTAACT
XM_005248001.4:c.*1919_*1926delinsCTCTAACT	XP_005248058.1:n.*1919_*1926delinsCTCTAACT
XM_005248002.3:c.*1919_*1926delinsCTCTAACT	XP_005248059.1:n.*1919_*1926delinsCTCTAACT
XM_011513557.2:c.*1919_*1926delinsCTCTAACT	XP_011511859.1:n.*1919_*1926delinsCTCTAACT
XM_011513560.2:c.*1919_*1926delinsCTCTAACT	XP_011511862.1:n.*1919_*1926delinsCTCTAACT
XM_017008587.1:c.*1919_*1926delinsCTCTAACT	XP_016864076.1:n.*1919_*1926delinsCTCTAACT
XM_017008588.1:c.*1919_*1926delinsCTCTAACT	XP_016864077.1:n.*1919_*1926delinsCTCTAACT
NM_001042424.3:c.*1919_*1926delinsCTCTAACT MANE Select	NP_001035889.1:n.*1919_*1926delinsCTCTAACT
NM_133330.3:c.*1919_*1926delinsCTCTAACT	NP_579877.1:n.*1919_*1926delinsCTCTAACT
NM_133331.3:c.*1919_*1926delinsCTCTAACT	NP_579878.1:n.*1919_*1926delinsCTCTAACT
NM_133335.4:c.*1919_*1926delinsCTCTAACT	NP_579890.1:n.*1919_*1926delinsCTCTAACT