Canonical Allele Identifier: CA7330700

Gene: DICER1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.95094011C>T , CM000676.2:g.95094011C>T	GRCh38
NC_000014.8:g.95560348C>T , CM000676.1:g.95560348C>T	GRCh37
NC_000014.7:g.94630101C>T	NCBI36
NG_016311.1:g.68412G>A , LRG_492:g.68412G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529720.2:c.5241G>A	ENSP00000433926.2:p.Ser1747=
ENST00000531162.7:c.5241G>A	ENSP00000433060.3:p.Ser1747=
ENST00000674628.2:c.5241G>A	ENSP00000502730.2:p.Ser1747=
ENST00000675540.2:c.*1891G>A	ENSP00000501988.2:n.*1891G>A
ENST00000696733.1:c.5241G>A	ENSP00000512838.1:p.Ser1747=
ENST00000696734.1:c.5241G>A	ENSP00000512839.1:p.Ser1747=
ENST00000696735.1:n.2228G>A
ENST00000696736.1:c.5241G>A	ENSP00000512840.1:p.Ser1747=
ENST00000696920.1:n.5504G>A
ENST00000696921.1:n.6347G>A
ENST00000696922.1:n.5650G>A
ENST00000696923.1:c.5241G>A	ENSP00000512976.1:p.Ser1747=
ENST00000696924.1:c.5241G>A	ENSP00000512977.1:p.Ser1747=
ENST00000696925.1:n.5650G>A
ENST00000343455.8:c.5241G>A MANE Select	ENSP00000343745.3:p.Ser1747=
ENST00000393063.6:c.5241G>A	ENSP00000376783.1:p.Ser1747=
ENST00000526495.6:c.5241G>A	ENSP00000437256.1:p.Ser1747=
ENST00000556045.6:c.5241G>A	ENSP00000451041.2:p.Ser1747=
ENST00000675540.1:c.2986G>A	ENSP00000501988.1:n.2986G>A
ENST00000675995.1:c.*3557G>A	ENSP00000502591.1:n.*3557G>A
ENST00000343455.7:c.5241G>A	ENSP00000343745.3:p.Ser1747=
ENST00000393063.5:c.5241G>A	ENSP00000376783.1:p.Ser1747=
ENST00000526495.5:c.5241G>A	ENSP00000437256.1:p.Ser1747=
ENST00000527414.5:c.5241G>A	ENSP00000435681.1:p.Ser1747=
ENST00000541352.5:c.5241G>A	ENSP00000444719.1:p.Ser1747=
ENST00000556045.5:c.1935G>A	ENSP00000451041.1:p.Ser645=
NM_001195573.1:c.5241G>A	NP_001182502.1:p.Ser1747=
NM_001271282.2:c.5241G>A	NP_001258211.1:p.Ser1747=
NM_001291628.1:c.5241G>A	NP_001278557.1:p.Ser1747=
NM_030621.4:c.5241G>A	NP_085124.2:p.Ser1747=
NM_177438.2:c.5241G>A , LRG_492t1:c.5241G>A	NP_803187.1:p.Ser1747=
XM_011536599.1:c.5241G>A	XP_011534901.1:p.Ser1747=
XM_011536600.1:c.5241G>A	XP_011534902.1:p.Ser1747=
XM_011536601.1:c.5241G>A	XP_011534903.1:p.Ser1747=
XM_011536602.1:c.5241G>A	XP_011534904.1:p.Ser1747=
XM_011536603.1:c.5241G>A	XP_011534905.1:p.Ser1747=
XM_011536604.1:c.4836G>A	XP_011534906.1:p.Ser1612=
XM_011536605.1:c.3762G>A	XP_011534907.1:p.Ser1254=
XM_011536599.2:c.5241G>A	XP_011534901.1:p.Ser1747=
XM_011536600.3:c.5241G>A	XP_011534902.1:p.Ser1747=
XM_011536601.3:c.5241G>A	XP_011534903.1:p.Ser1747=
XM_011536602.3:c.5241G>A	XP_011534904.1:p.Ser1747=
XM_011536604.2:c.4836G>A	XP_011534906.1:p.Ser1612=
XM_011536605.2:c.3762G>A	XP_011534907.1:p.Ser1254=
XM_017021120.2:c.5241G>A	XP_016876609.1:p.Ser1747=
XM_017021121.2:c.5241G>A	XP_016876610.1:p.Ser1747=
XM_017021122.2:c.4836G>A	XP_016876611.1:p.Ser1612=
XM_017021123.2:c.4836G>A	XP_016876612.1:p.Ser1612=
NM_001271282.3:c.5241G>A	NP_001258211.1:p.Ser1747=
NM_001291628.2:c.5241G>A	NP_001278557.1:p.Ser1747=
NM_177438.3:c.5241G>A MANE Select	NP_803187.1:p.Ser1747=
NM_001395677.1:c.5241G>A	NP_001382606.1:p.Ser1747=
NM_001395678.1:c.5241G>A	NP_001382607.1:p.Ser1747=
NM_001395679.1:c.5241G>A	NP_001382608.1:p.Ser1747=
NM_001395680.1:c.5241G>A	NP_001382609.1:p.Ser1747=
NM_001395682.1:c.5241G>A	NP_001382611.1:p.Ser1747=
NM_001395683.1:c.5241G>A	NP_001382612.1:p.Ser1747=
NM_001395684.1:c.5241G>A	NP_001382613.1:p.Ser1747=
NM_001395685.1:c.5241G>A	NP_001382614.1:p.Ser1747=
NM_001395686.1:c.4959G>A	NP_001382615.1:p.Ser1653=
NM_001395687.1:c.4836G>A	NP_001382616.1:p.Ser1612=
NM_001395688.1:c.4836G>A	NP_001382617.1:p.Ser1612=
NM_001395689.1:c.4836G>A	NP_001382618.1:p.Ser1612=
NM_001395690.1:c.4836G>A	NP_001382619.1:p.Ser1612=
NM_001395691.1:c.4674G>A	NP_001382620.1:p.Ser1558=
NM_001395697.1:c.3558G>A	NP_001382626.1:p.Ser1186=
NR_172715.1:n.5659G>A
NR_172716.1:n.5843G>A
NR_172717.1:n.5753G>A
NR_172718.1:n.5676G>A
NR_172719.1:n.5509G>A
NR_172720.1:n.5586G>A