Canonical Allele Identifier: CA7330596
Gene: DICER1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.95090506T>G , CM000676.2:g.95090506T>G GRCh38
NC_000014.8:g.95556843T>G , CM000676.1:g.95556843T>G GRCh37
NC_000014.7:g.94626596T>G NCBI36
NG_016311.1:g.71917A>C , LRG_492:g.71917A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000529720.2:c.5761A>C ENSP00000433926.2:p.Asn1921His
ENST00000531162.7:c.5761A>C ENSP00000433060.3:p.Asn1921His
ENST00000674628.2:c.5761A>C ENSP00000502730.2:p.Asn1921His
ENST00000675540.2:c.*2411A>C ENSP00000501988.2:n.*2411A>C
ENST00000696733.1:c.*383A>C ENSP00000512838.1:n.*383A>C
ENST00000696734.1:c.*416A>C ENSP00000512839.1:n.*416A>C
ENST00000696735.1:n.2748A>C
ENST00000696920.1:n.6024A>C
ENST00000696921.1:n.6867A>C
ENST00000696922.1:n.8692A>C
ENST00000696923.1:c.*416A>C ENSP00000512976.1:n.*416A>C
ENST00000696924.1:c.*383A>C ENSP00000512977.1:n.*383A>C
ENST00000696925.1:n.9062A>C
ENST00000343455.8:c.5761A>C MANE Select ENSP00000343745.3:p.Asn1921His
ENST00000393063.6:c.5761A>C ENSP00000376783.1:p.Asn1921His
ENST00000526495.6:c.5761A>C ENSP00000437256.1:p.Asn1921His
ENST00000556045.6:c.*478A>C ENSP00000451041.2:n.*478A>C
ENST00000675540.1:c.3506A>C ENSP00000501988.1:n.3506A>C
ENST00000675995.1:c.*4077A>C ENSP00000502591.1:n.*4077A>C
ENST00000343455.7:c.5761A>C ENSP00000343745.3:p.Asn1921His
ENST00000393063.5:c.5761A>C ENSP00000376783.1:p.Asn1921His
ENST00000526495.5:c.5761A>C ENSP00000437256.1:p.Asn1921His
ENST00000527414.5:c.5761A>C ENSP00000435681.1:p.Asn1921His
ENST00000527416.2:n.347+7A>C
ENST00000541352.5:c.*108A>C ENSP00000444719.1:n.*108A>C
ENST00000556045.5:c.2455A>C ENSP00000451041.1:p.Asn819His
NM_001195573.1:c.*108A>C NP_001182502.1:n.*108A>C
NM_001271282.2:c.5761A>C NP_001258211.1:p.Asn1921His
NM_001291628.1:c.5761A>C NP_001278557.1:p.Asn1921His
NM_030621.4:c.5761A>C NP_085124.2:p.Asn1921His
NM_177438.2:c.5761A>C , LRG_492t1:c.5761A>C NP_803187.1:p.Asn1921His
XM_011536599.1:c.5761A>C XP_011534901.1:p.Asn1921His
XM_011536600.1:c.5761A>C XP_011534902.1:p.Asn1921His
XM_011536601.1:c.5761A>C XP_011534903.1:p.Asn1921His
XM_011536602.1:c.5761A>C XP_011534904.1:p.Asn1921His
XM_011536603.1:c.5761A>C XP_011534905.1:p.Asn1921His
XM_011536604.1:c.5356A>C XP_011534906.1:p.Asn1786His
XM_011536605.1:c.4282A>C XP_011534907.1:p.Asn1428His
XM_011536599.2:c.5761A>C XP_011534901.1:p.Asn1921His
XM_011536600.3:c.5761A>C XP_011534902.1:p.Asn1921His
XM_011536601.3:c.5761A>C XP_011534903.1:p.Asn1921His
XM_011536602.3:c.5761A>C XP_011534904.1:p.Asn1921His
XM_011536604.2:c.5356A>C XP_011534906.1:p.Asn1786His
XM_011536605.2:c.4282A>C XP_011534907.1:p.Asn1428His
XM_017021120.2:c.5761A>C XP_016876609.1:p.Asn1921His
XM_017021121.2:c.5761A>C XP_016876610.1:p.Asn1921His
XM_017021122.2:c.5356A>C XP_016876611.1:p.Asn1786His
XM_017021123.2:c.5356A>C XP_016876612.1:p.Asn1786His
NM_001271282.3:c.5761A>C NP_001258211.1:p.Asn1921His
NM_001291628.2:c.5761A>C NP_001278557.1:p.Asn1921His
NM_177438.3:c.5761A>C MANE Select NP_803187.1:p.Asn1921His
NM_001395677.1:c.5761A>C NP_001382606.1:p.Asn1921His
NM_001395678.1:c.5761A>C NP_001382607.1:p.Asn1921His
NM_001395679.1:c.5761A>C NP_001382608.1:p.Asn1921His
NM_001395680.1:c.5761A>C NP_001382609.1:p.Asn1921His
NM_001395682.1:c.5761A>C NP_001382611.1:p.Asn1921His
NM_001395683.1:c.5761A>C NP_001382612.1:p.Asn1921His
NM_001395684.1:c.5761A>C NP_001382613.1:p.Asn1921His
NM_001395685.1:c.*307A>C NP_001382614.1:n.*307A>C
NM_001395686.1:c.5479A>C NP_001382615.1:p.Asn1827His
NM_001395687.1:c.5356A>C NP_001382616.1:p.Asn1786His
NM_001395688.1:c.5356A>C NP_001382617.1:p.Asn1786His
NM_001395689.1:c.5356A>C NP_001382618.1:p.Asn1786His
NM_001395690.1:c.5356A>C NP_001382619.1:p.Asn1786His
NM_001395691.1:c.5194A>C NP_001382620.1:p.Asn1732His
NM_001395697.1:c.4078A>C NP_001382626.1:p.Asn1360His
NR_172715.1:n.6172+7A>C
NR_172716.1:n.6363A>C
NR_172717.1:n.6266+7A>C
NR_172718.1:n.6196A>C
NR_172719.1:n.6029A>C
NR_172720.1:n.6232A>C