Canonical Allele Identifier: CA792740118
Gene: NSD2 HGNC NCBI

Linked Data

dbSNP Id: rs1427317707
gnomAD v3: 4-1981069-G-A
gnomAD v4: 4-1981069-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1981069G>A , CM000666.2:g.1981069G>A GRCh38
NC_000004.11:g.1982796G>A , CM000666.1:g.1982796G>A GRCh37
NC_000004.10:g.1952594G>A NCBI36
NG_009232.1:g.33164C>T
NG_009269.1:g.114674G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000508803.6:c.*2160G>A MANE Select ENSP00000423972.1:n.*2160G>A
ENST00000677559.1:c.*4024G>A ENSP00000504406.1:n.*4024G>A
ENST00000677895.1:c.*2160G>A ENSP00000503076.1:n.*2160G>A
ENST00000679039.1:n.3448G>A
ENST00000312087.10:c.*4541G>A ENSP00000308780.6:n.*4541G>A
ENST00000353275.9:c.*4408G>A ENSP00000329167.5:n.*4408G>A
ENST00000382891.9:c.*2160G>A ENSP00000372347.5:n.*2160G>A
ENST00000382892.6:c.*2160G>A ENSP00000372348.2:n.*2160G>A
ENST00000382895.7:c.*2160G>A ENSP00000372351.3:n.*2160G>A
NM_001042424.2:c.*2160G>A NP_001035889.1:n.*2160G>A
NM_133330.2:c.*2160G>A NP_579877.1:n.*2160G>A
NM_133331.2:c.*2160G>A NP_579878.1:n.*2160G>A
NM_133335.3:c.*2160G>A NP_579890.1:n.*2160G>A
XM_005248001.3:c.*2160G>A XP_005248058.1:n.*2160G>A
XM_005248002.1:c.*2160G>A XP_005248059.1:n.*2160G>A
XM_006713915.2:c.*2160G>A XP_006713978.1:n.*2160G>A
XM_011513557.1:c.*2160G>A XP_011511859.1:n.*2160G>A
XM_011513558.1:c.*2160G>A XP_011511860.1:n.*2160G>A
XM_011513559.1:c.*2160G>A XP_011511861.1:n.*2160G>A
XM_011513560.1:c.*2160G>A XP_011511862.1:n.*2160G>A
XM_005248001.4:c.*2160G>A XP_005248058.1:n.*2160G>A
XM_005248002.3:c.*2160G>A XP_005248059.1:n.*2160G>A
XM_011513557.2:c.*2160G>A XP_011511859.1:n.*2160G>A
XM_011513560.2:c.*2160G>A XP_011511862.1:n.*2160G>A
XM_017008587.1:c.*2160G>A XP_016864076.1:n.*2160G>A
XM_017008588.1:c.*2160G>A XP_016864077.1:n.*2160G>A
NM_001042424.3:c.*2160G>A MANE Select NP_001035889.1:n.*2160G>A
NM_133330.3:c.*2160G>A NP_579877.1:n.*2160G>A
NM_133331.3:c.*2160G>A NP_579878.1:n.*2160G>A
NM_133335.4:c.*2160G>A NP_579890.1:n.*2160G>A