Canonical Allele Identifier: CA2156299219
Community Standard Title: NM_177438.3(DICER1):c.*3473T=
Gene: DICER1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.95087025A= , CM000676.2:g.95087025A= GRCh38
NC_000014.8:g.95553362A= , CM000676.1:g.95553362A= GRCh37
NC_000014.7:g.94623115A= NCBI36
NG_016311.1:g.75398T= , LRG_492:g.75398T=

Transcript Alleles

HGVS Amino-acid Change
NM_177438.3:c.*3473T= MANE Select NP_803187.1:n.*3473T=
ENST00000343455.8:c.*3473T= MANE Select ENSP00000343745.3:n.*3473T=
NM_001195573.1:c.*3589T= NP_001182502.1:n.*3589T=
NM_001271282.2:c.*3473T= NP_001258211.1:n.*3473T=
NM_001271282.3:c.*3473T= NP_001258211.1:n.*3473T=
NM_001291628.1:c.*3473T= NP_001278557.1:n.*3473T=
NM_001291628.2:c.*3473T= NP_001278557.1:n.*3473T=
NM_001395677.1:c.*3473T= NP_001382606.1:n.*3473T=
NM_001395678.1:c.*3473T= NP_001382607.1:n.*3473T=
NM_001395679.1:c.*3473T= NP_001382608.1:n.*3473T=
NM_001395680.1:c.*3473T= NP_001382609.1:n.*3473T=
NM_001395682.1:c.*3473T= NP_001382611.1:n.*3473T=
NM_001395683.1:c.*3473T= NP_001382612.1:n.*3473T=
NM_001395684.1:c.*3473T= NP_001382613.1:n.*3473T=
NM_001395685.1:c.*3788T= NP_001382614.1:n.*3788T=
NM_001395686.1:c.*3473T= NP_001382615.1:n.*3473T=
NM_001395687.1:c.*3473T= NP_001382616.1:n.*3473T=
NM_001395688.1:c.*3473T= NP_001382617.1:n.*3473T=
NM_001395689.1:c.*3473T= NP_001382618.1:n.*3473T=
NM_001395690.1:c.*3473T= NP_001382619.1:n.*3473T=
NM_001395691.1:c.*3473T= NP_001382620.1:n.*3473T=
NM_001395697.1:c.*3473T= NP_001382626.1:n.*3473T=
NM_030621.4:c.*3473T= NP_085124.2:n.*3473T=
NM_177438.2:c.*3473T= , LRG_492t1:c.*3473T= NP_803187.1:n.*3473T=
NR_172715.1:n.6537T=
NR_172716.1:n.9844T=
NR_172717.1:n.6631T=
NR_172718.1:n.9677T=
NR_172719.1:n.9510T=
NR_172720.1:n.9713T=
ENST00000343455.7:c.*3473T= ENSP00000343745.3:n.*3473T=
ENST00000393063.5:c.*3473T= ENSP00000376783.1:n.*3473T=
ENST00000526495.5:c.*3473T= ENSP00000437256.1:n.*3473T=
ENST00000526495.6:c.*3473T= ENSP00000437256.1:n.*3473T=
ENST00000529720.2:c.*3473T= ENSP00000433926.2:n.*3473T=
ENST00000531162.7:c.*3473T= ENSP00000433060.3:n.*3473T=
ENST00000674628.2:c.*3473T= ENSP00000502730.2:n.*3473T=
ENST00000675540.1:c.6987T= ENSP00000501988.1:n.6987T=
ENST00000675540.2:c.*5892T= ENSP00000501988.2:n.*5892T=
ENST00000696733.1:c.*3864T= ENSP00000512838.1:n.*3864T=
ENST00000696734.1:c.*3897T= ENSP00000512839.1:n.*3897T=
ENST00000696920.1:n.9505T=
ENST00000696921.1:n.10348T=
ENST00000696922.1:n.12173T=
ENST00000696923.1:c.*3897T= ENSP00000512976.1:n.*3897T=
ENST00000696924.1:c.*3864T= ENSP00000512977.1:n.*3864T=
XM_011536599.1:c.*3473T= XP_011534901.1:n.*3473T=
XM_011536599.2:c.*3473T= XP_011534901.1:n.*3473T=
XM_011536600.1:c.*3473T= XP_011534902.1:n.*3473T=
XM_011536600.3:c.*3473T= XP_011534902.1:n.*3473T=
XM_011536601.1:c.*3473T= XP_011534903.1:n.*3473T=
XM_011536601.3:c.*3473T= XP_011534903.1:n.*3473T=
XM_011536602.1:c.*3473T= XP_011534904.1:n.*3473T=
XM_011536602.3:c.*3473T= XP_011534904.1:n.*3473T=
XM_011536603.1:c.*3473T= XP_011534905.1:n.*3473T=
XM_011536604.1:c.*3473T= XP_011534906.1:n.*3473T=
XM_011536604.2:c.*3473T= XP_011534906.1:n.*3473T=
XM_011536605.1:c.*3473T= XP_011534907.1:n.*3473T=
XM_011536605.2:c.*3473T= XP_011534907.1:n.*3473T=
XM_017021120.2:c.*3473T= XP_016876609.1:n.*3473T=
XM_017021121.2:c.*3473T= XP_016876610.1:n.*3473T=
XM_017021122.2:c.*3473T= XP_016876611.1:n.*3473T=
XM_017021123.2:c.*3473T= XP_016876612.1:n.*3473T=