Canonical Allele Identifier: CA2580616056
Gene: NSD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1918576_1918577dup , CM000666.2:g.1918576_1918577dup GRCh38
NC_000004.11:g.1920303_1920304dup , CM000666.1:g.1920303_1920304dup GRCh37
NC_000004.10:g.1890101_1890102dup NCBI36
NG_009269.1:g.52181_52182dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000398261.6:c.1363_1364dup ENSP00000381311.1:p.Asp455GlufsTer19
ENST00000508803.6:c.1363_1364dup MANE Select ENSP00000423972.1:p.Asp455GlufsTer19
ENST00000512700.2:c.1363_1364dup ENSP00000427516.2:p.Asp455GlufsTer19
ENST00000677559.1:c.1363_1364dup ENSP00000504406.1:p.Asp455GlufsTer19
ENST00000678714.1:c.*645_*646dup ENSP00000504221.1:n.*645_*646dup
ENST00000312087.10:c.1363_1364dup ENSP00000308780.6:p.Asp455GlufsTer19
ENST00000353275.9:c.1363_1364dup ENSP00000329167.5:p.Asp455GlufsTer19
ENST00000382891.9:c.1363_1364dup ENSP00000372347.5:p.Asp455GlufsTer19
ENST00000382892.6:c.1363_1364dup ENSP00000372348.2:p.Asp455GlufsTer19
ENST00000382895.7:c.1363_1364dup ENSP00000372351.3:p.Asp455GlufsTer19
ENST00000398261.5:c.1363_1364dup ENSP00000381311.1:p.Asp455GlufsTer19
ENST00000420906.6:c.1363_1364dup ENSP00000399251.2:p.Asp455GlufsTer19
ENST00000503128.5:c.1363_1364dup ENSP00000425761.1:p.Asp455GlufsTer19
ENST00000508355.5:n.1481_1482dup
ENST00000508803.5:c.1363_1364dup ENSP00000423972.1:p.Asp455GlufsTer19
ENST00000511904.1:c.145_146dup ENSP00000424482.1:p.Asp49GlufsTer19
ENST00000514045.5:c.1363_1364dup ENSP00000421681.1:p.Asp455GlufsTer19
NM_001042424.2:c.1363_1364dup NP_001035889.1:p.Asp455GlufsTer19
NM_007331.1:c.1363_1364dup NP_015627.1:p.Asp455GlufsTer19
NM_133330.2:c.1363_1364dup NP_579877.1:p.Asp455GlufsTer19
NM_133331.2:c.1363_1364dup NP_579878.1:p.Asp455GlufsTer19
NM_133334.2:c.1363_1364dup NP_579889.1:p.Asp455GlufsTer19
NM_133335.3:c.1363_1364dup NP_579890.1:p.Asp455GlufsTer19
XM_005248001.3:c.1363_1364dup XP_005248058.1:p.Asp455GlufsTer19
XM_005248002.1:c.1363_1364dup XP_005248059.1:p.Asp455GlufsTer19
XM_005248005.1:c.1363_1364dup XP_005248062.1:p.Asp455GlufsTer19
XM_006713914.2:c.1363_1364dup XP_006713977.1:p.Asp455GlufsTer19
XM_011513557.1:c.1363_1364dup XP_011511859.1:p.Asp455GlufsTer19
XM_011513558.1:c.1363_1364dup XP_011511860.1:p.Asp455GlufsTer19
XM_005248001.4:c.1363_1364dup XP_005248058.1:p.Asp455GlufsTer19
XM_005248002.3:c.1363_1364dup XP_005248059.1:p.Asp455GlufsTer19
XM_005248005.3:c.1363_1364dup XP_005248062.1:p.Asp455GlufsTer19
XM_006713914.3:c.1363_1364dup XP_006713977.1:p.Asp455GlufsTer19
XM_011513557.2:c.1363_1364dup XP_011511859.1:p.Asp455GlufsTer19
NM_001042424.3:c.1363_1364dup MANE Select NP_001035889.1:p.Asp455GlufsTer19
NM_007331.2:c.1363_1364dup NP_015627.1:p.Asp455GlufsTer19
NM_133330.3:c.1363_1364dup NP_579877.1:p.Asp455GlufsTer19
NM_133331.3:c.1363_1364dup NP_579878.1:p.Asp455GlufsTer19
NM_133335.4:c.1363_1364dup NP_579890.1:p.Asp455GlufsTer19