Canonical Allele Identifier: CA10635595

Gene: DICER1

Linked Data

• ClinVar Variation Id: 315043
• ClinVar RCV Id: RCV000390820
• dbSNP Id: rs886050926
• gnomAD v3: 14-95086238-A-G
• gnomAD v4: 14-95086238-A-G
• MyVariant Identifiers: chr14:g.95552575A>G (hg19) ; chr14:g.95086238A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.95086238A>G , CM000676.2:g.95086238A>G	GRCh38
NC_000014.8:g.95552575A>G , CM000676.1:g.95552575A>G	GRCh37
NC_000014.7:g.94622328A>G	NCBI36
NG_016311.1:g.76185T>C , LRG_492:g.76185T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000529720.2:c.*4260T>C	ENSP00000433926.2:n.*4260T>C
ENST00000674628.2:c.*4260T>C	ENSP00000502730.2:n.*4260T>C
ENST00000343455.8:c.*4260T>C MANE Select	ENSP00000343745.3:n.*4260T>C
ENST00000343455.7:c.*4260T>C	ENSP00000343745.3:n.*4260T>C
ENST00000393063.5:c.*4260T>C	ENSP00000376783.1:n.*4260T>C
ENST00000526495.5:c.*4260T>C	ENSP00000437256.1:n.*4260T>C
NM_001195573.1:c.*4376T>C	NP_001182502.1:n.*4376T>C
NM_001271282.2:c.*4260T>C	NP_001258211.1:n.*4260T>C
NM_001291628.1:c.*4260T>C	NP_001278557.1:n.*4260T>C
NM_030621.4:c.*4260T>C	NP_085124.2:n.*4260T>C
NM_177438.2:c.*4260T>C , LRG_492t1:c.*4260T>C	NP_803187.1:n.*4260T>C
XM_011536599.1:c.*4260T>C	XP_011534901.1:n.*4260T>C
XM_011536600.1:c.*4260T>C	XP_011534902.1:n.*4260T>C
XM_011536601.1:c.*4260T>C	XP_011534903.1:n.*4260T>C
XM_011536602.1:c.*4260T>C	XP_011534904.1:n.*4260T>C
XM_011536603.1:c.*4260T>C	XP_011534905.1:n.*4260T>C
XM_011536604.1:c.*4260T>C	XP_011534906.1:n.*4260T>C
XM_011536605.1:c.*4260T>C	XP_011534907.1:n.*4260T>C
XM_011536599.2:c.*4260T>C	XP_011534901.1:n.*4260T>C
XM_011536600.3:c.*4260T>C	XP_011534902.1:n.*4260T>C
XM_011536601.3:c.*4260T>C	XP_011534903.1:n.*4260T>C
XM_011536602.3:c.*4260T>C	XP_011534904.1:n.*4260T>C
XM_017021120.2:c.*4260T>C	XP_016876609.1:n.*4260T>C
XM_017021121.2:c.*4260T>C	XP_016876610.1:n.*4260T>C
NM_001271282.3:c.*4260T>C	NP_001258211.1:n.*4260T>C
NM_001291628.2:c.*4260T>C	NP_001278557.1:n.*4260T>C
NM_177438.3:c.*4260T>C MANE Select	NP_803187.1:n.*4260T>C
NM_001395677.1:c.*4260T>C	NP_001382606.1:n.*4260T>C
NM_001395678.1:c.*4260T>C	NP_001382607.1:n.*4260T>C
NM_001395679.1:c.*4260T>C	NP_001382608.1:n.*4260T>C
NM_001395680.1:c.*4260T>C	NP_001382609.1:n.*4260T>C
NM_001395682.1:c.*4260T>C	NP_001382611.1:n.*4260T>C
NM_001395683.1:c.*4260T>C	NP_001382612.1:n.*4260T>C
NM_001395684.1:c.*4260T>C	NP_001382613.1:n.*4260T>C
NM_001395685.1:c.*4575T>C	NP_001382614.1:n.*4575T>C
NM_001395686.1:c.*4260T>C	NP_001382615.1:n.*4260T>C
NM_001395687.1:c.*4260T>C	NP_001382616.1:n.*4260T>C
NM_001395688.1:c.*4260T>C	NP_001382617.1:n.*4260T>C
NM_001395689.1:c.*4260T>C	NP_001382618.1:n.*4260T>C
NM_001395690.1:c.*4260T>C	NP_001382619.1:n.*4260T>C
NM_001395691.1:c.*4260T>C	NP_001382620.1:n.*4260T>C
NM_001395697.1:c.*4260T>C	NP_001382626.1:n.*4260T>C
NR_172715.1:n.7324T>C
NR_172716.1:n.10631T>C
NR_172717.1:n.7418T>C
NR_172718.1:n.10464T>C
NR_172719.1:n.10297T>C
NR_172720.1:n.10500T>C