Canonical Allele Identifier: CA549205181
Gene: NSD2 HGNC NCBI

Linked Data

dbSNP Id: rs1171046467
gnomAD v2: 4-1982540-GC-G
gnomAD v3: 4-1980813-GC-G
gnomAD v4: 4-1980813-GC-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1980814del , CM000666.2:g.1980814del GRCh38
NC_000004.11:g.1982541del , CM000666.1:g.1982541del GRCh37
NC_000004.10:g.1952339del NCBI36
NG_009232.1:g.33419del
NG_009269.1:g.114419del

Transcript Alleles

HGVS Amino-acid Change
ENST00000508803.6:c.*1905del MANE Select ENSP00000423972.1:n.*1905del
ENST00000677559.1:c.*3769del ENSP00000504406.1:n.*3769del
ENST00000677895.1:c.*1905del ENSP00000503076.1:n.*1905del
ENST00000679039.1:n.3193del
ENST00000312087.10:c.*4286del ENSP00000308780.6:n.*4286del
ENST00000353275.9:c.*4153del ENSP00000329167.5:n.*4153del
ENST00000382891.9:c.*1905del ENSP00000372347.5:n.*1905del
ENST00000382892.6:c.*1905del ENSP00000372348.2:n.*1905del
ENST00000382895.7:c.*1905del ENSP00000372351.3:n.*1905del
NM_001042424.2:c.*1905del NP_001035889.1:n.*1905del
NM_133330.2:c.*1905del NP_579877.1:n.*1905del
NM_133331.2:c.*1905del NP_579878.1:n.*1905del
NM_133335.3:c.*1905del NP_579890.1:n.*1905del
XM_005248001.3:c.*1905del XP_005248058.1:n.*1905del
XM_005248002.1:c.*1905del XP_005248059.1:n.*1905del
XM_006713915.2:c.*1905del XP_006713978.1:n.*1905del
XM_011513557.1:c.*1905del XP_011511859.1:n.*1905del
XM_011513558.1:c.*1905del XP_011511860.1:n.*1905del
XM_011513559.1:c.*1905del XP_011511861.1:n.*1905del
XM_011513560.1:c.*1905del XP_011511862.1:n.*1905del
XM_005248001.4:c.*1905del XP_005248058.1:n.*1905del
XM_005248002.3:c.*1905del XP_005248059.1:n.*1905del
XM_011513557.2:c.*1905del XP_011511859.1:n.*1905del
XM_011513560.2:c.*1905del XP_011511862.1:n.*1905del
XM_017008587.1:c.*1905del XP_016864076.1:n.*1905del
XM_017008588.1:c.*1905del XP_016864077.1:n.*1905del
NM_001042424.3:c.*1905del MANE Select NP_001035889.1:n.*1905del
NM_133330.3:c.*1905del NP_579877.1:n.*1905del
NM_133331.3:c.*1905del NP_579878.1:n.*1905del
NM_133335.4:c.*1905del NP_579890.1:n.*1905del