Canonical Allele Identifier: CA1433597835
Gene: NSD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1980722C= , CM000666.2:g.1980722C= GRCh38
NC_000004.11:g.1982449C= , CM000666.1:g.1982449C= GRCh37
NC_000004.10:g.1952247C= NCBI36
NG_009232.1:g.33511G=
NG_009269.1:g.114327C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000508803.6:c.*1813C= MANE Select ENSP00000423972.1:n.*1813C=
ENST00000677559.1:c.*3677C= ENSP00000504406.1:n.*3677C=
ENST00000677895.1:c.*1813C= ENSP00000503076.1:n.*1813C=
ENST00000679039.1:n.3101C=
ENST00000312087.10:c.*4194C= ENSP00000308780.6:n.*4194C=
ENST00000353275.9:c.*4061C= ENSP00000329167.5:n.*4061C=
ENST00000382891.9:c.*1813C= ENSP00000372347.5:n.*1813C=
ENST00000382892.6:c.*1813C= ENSP00000372348.2:n.*1813C=
ENST00000382895.7:c.*1813C= ENSP00000372351.3:n.*1813C=
NM_001042424.2:c.*1813C= NP_001035889.1:n.*1813C=
NM_133330.2:c.*1813C= NP_579877.1:n.*1813C=
NM_133331.2:c.*1813C= NP_579878.1:n.*1813C=
NM_133335.3:c.*1813C= NP_579890.1:n.*1813C=
XM_005248001.3:c.*1813C= XP_005248058.1:n.*1813C=
XM_005248002.1:c.*1813C= XP_005248059.1:n.*1813C=
XM_006713915.2:c.*1813C= XP_006713978.1:n.*1813C=
XM_011513557.1:c.*1813C= XP_011511859.1:n.*1813C=
XM_011513558.1:c.*1813C= XP_011511860.1:n.*1813C=
XM_011513559.1:c.*1813C= XP_011511861.1:n.*1813C=
XM_011513560.1:c.*1813C= XP_011511862.1:n.*1813C=
XM_005248001.4:c.*1813C= XP_005248058.1:n.*1813C=
XM_005248002.3:c.*1813C= XP_005248059.1:n.*1813C=
XM_011513557.2:c.*1813C= XP_011511859.1:n.*1813C=
XM_011513560.2:c.*1813C= XP_011511862.1:n.*1813C=
XM_017008587.1:c.*1813C= XP_016864076.1:n.*1813C=
XM_017008588.1:c.*1813C= XP_016864077.1:n.*1813C=
NM_001042424.3:c.*1813C= MANE Select NP_001035889.1:n.*1813C=
NM_133330.3:c.*1813C= NP_579877.1:n.*1813C=
NM_133331.3:c.*1813C= NP_579878.1:n.*1813C=
NM_133335.4:c.*1813C= NP_579890.1:n.*1813C=