Canonical Allele Identifier: CA487843671
Gene: DICER1 HGNC NCBI

Linked Data

ClinVar Variation Id: 477262
dbSNP Id: rs1555366154

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.95091209G>A , CM000676.2:g.95091209G>A GRCh38
NC_000014.8:g.95557546G>A , CM000676.1:g.95557546G>A GRCh37
NC_000014.7:g.94627299G>A NCBI36
NG_016311.1:g.71214C>T , LRG_492:g.71214C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000529720.2:c.5521C>T ENSP00000433926.2:p.Leu1841=
ENST00000531162.7:c.5521C>T ENSP00000433060.3:p.Leu1841=
ENST00000674628.2:c.5521C>T ENSP00000502730.2:p.Leu1841=
ENST00000675540.2:c.*2171C>T ENSP00000501988.2:n.*2171C>T
ENST00000696733.1:c.*143C>T ENSP00000512838.1:n.*143C>T
ENST00000696734.1:c.*176C>T ENSP00000512839.1:n.*176C>T
ENST00000696735.1:n.2508C>T
ENST00000696736.1:c.5521C>T ENSP00000512840.1:p.Leu1841=
ENST00000696920.1:n.5784C>T
ENST00000696921.1:n.6627C>T
ENST00000696922.1:n.8452C>T
ENST00000696923.1:c.*176C>T ENSP00000512976.1:n.*176C>T
ENST00000696924.1:c.*143C>T ENSP00000512977.1:n.*143C>T
ENST00000696925.1:n.8452C>T
ENST00000343455.8:c.5521C>T MANE Select ENSP00000343745.3:p.Leu1841=
ENST00000393063.6:c.5521C>T ENSP00000376783.1:p.Leu1841=
ENST00000526495.6:c.5521C>T ENSP00000437256.1:p.Leu1841=
ENST00000556045.6:c.*238C>T ENSP00000451041.2:n.*238C>T
ENST00000675540.1:c.3266C>T ENSP00000501988.1:n.3266C>T
ENST00000675995.1:c.*3837C>T ENSP00000502591.1:n.*3837C>T
ENST00000343455.7:c.5521C>T ENSP00000343745.3:p.Leu1841=
ENST00000393063.5:c.5521C>T ENSP00000376783.1:p.Leu1841=
ENST00000526495.5:c.5521C>T ENSP00000437256.1:p.Leu1841=
ENST00000527414.5:c.5521C>T ENSP00000435681.1:p.Leu1841=
ENST00000527416.2:n.114C>T
ENST00000527554.2:n.214C>T
ENST00000541352.5:c.5365-100C>T ENSP00000444719.1:n.5365-100C>T
ENST00000556045.5:c.2215C>T ENSP00000451041.1:p.Leu739=
NM_001195573.1:c.5365-100C>T NP_001182502.1:n.5365-100C>T
NM_001271282.2:c.5521C>T NP_001258211.1:p.Leu1841=
NM_001291628.1:c.5521C>T NP_001278557.1:p.Leu1841=
NM_030621.4:c.5521C>T NP_085124.2:p.Leu1841=
NM_177438.2:c.5521C>T , LRG_492t1:c.5521C>T NP_803187.1:p.Leu1841=
XM_011536599.1:c.5521C>T XP_011534901.1:p.Leu1841=
XM_011536600.1:c.5521C>T XP_011534902.1:p.Leu1841=
XM_011536601.1:c.5521C>T XP_011534903.1:p.Leu1841=
XM_011536602.1:c.5521C>T XP_011534904.1:p.Leu1841=
XM_011536603.1:c.5521C>T XP_011534905.1:p.Leu1841=
XM_011536604.1:c.5116C>T XP_011534906.1:p.Leu1706=
XM_011536605.1:c.4042C>T XP_011534907.1:p.Leu1348=
XM_011536599.2:c.5521C>T XP_011534901.1:p.Leu1841=
XM_011536600.3:c.5521C>T XP_011534902.1:p.Leu1841=
XM_011536601.3:c.5521C>T XP_011534903.1:p.Leu1841=
XM_011536602.3:c.5521C>T XP_011534904.1:p.Leu1841=
XM_011536604.2:c.5116C>T XP_011534906.1:p.Leu1706=
XM_011536605.2:c.4042C>T XP_011534907.1:p.Leu1348=
XM_017021120.2:c.5521C>T XP_016876609.1:p.Leu1841=
XM_017021121.2:c.5521C>T XP_016876610.1:p.Leu1841=
XM_017021122.2:c.5116C>T XP_016876611.1:p.Leu1706=
XM_017021123.2:c.5116C>T XP_016876612.1:p.Leu1706=
NM_001271282.3:c.5521C>T NP_001258211.1:p.Leu1841=
NM_001291628.2:c.5521C>T NP_001278557.1:p.Leu1841=
NM_177438.3:c.5521C>T MANE Select NP_803187.1:p.Leu1841=
NM_001395677.1:c.5521C>T NP_001382606.1:p.Leu1841=
NM_001395678.1:c.5521C>T NP_001382607.1:p.Leu1841=
NM_001395679.1:c.5521C>T NP_001382608.1:p.Leu1841=
NM_001395680.1:c.5521C>T NP_001382609.1:p.Leu1841=
NM_001395682.1:c.5521C>T NP_001382611.1:p.Leu1841=
NM_001395683.1:c.5521C>T NP_001382612.1:p.Leu1841=
NM_001395684.1:c.5521C>T NP_001382613.1:p.Leu1841=
NM_001395685.1:c.5521C>T NP_001382614.1:p.Leu1841=
NM_001395686.1:c.5239C>T NP_001382615.1:p.Leu1747=
NM_001395687.1:c.5116C>T NP_001382616.1:p.Leu1706=
NM_001395688.1:c.5116C>T NP_001382617.1:p.Leu1706=
NM_001395689.1:c.5116C>T NP_001382618.1:p.Leu1706=
NM_001395690.1:c.5116C>T NP_001382619.1:p.Leu1706=
NM_001395691.1:c.4954C>T NP_001382620.1:p.Leu1652=
NM_001395697.1:c.3838C>T NP_001382626.1:p.Leu1280=
NR_172715.1:n.5939C>T
NR_172716.1:n.6123C>T
NR_172717.1:n.6033C>T
NR_172718.1:n.5956C>T
NR_172719.1:n.5789C>T
NR_172720.1:n.5992C>T