Canonical Allele Identifier: CA265893085

Gene: DICER1

Linked Data

• dbSNP Id: rs141919532
• gnomAD v2: 14-95554173-G-A
• gnomAD v3: 14-95087836-G-A
• gnomAD v4: 14-95087836-G-A
• MyVariant Identifiers: chr14:g.95554173G>A (hg19) ; chr14:g.95087836G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.95087836G>A , CM000676.2:g.95087836G>A	GRCh38
NC_000014.8:g.95554173G>A , CM000676.1:g.95554173G>A	GRCh37
NC_000014.7:g.94623926G>A	NCBI36
NG_016311.1:g.74587C>T , LRG_492:g.74587C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000529720.2:c.*2662C>T	ENSP00000433926.2:n.*2662C>T
ENST00000531162.7:c.*2662C>T	ENSP00000433060.3:n.*2662C>T
ENST00000674628.2:c.*2662C>T	ENSP00000502730.2:n.*2662C>T
ENST00000675540.2:c.*5081C>T	ENSP00000501988.2:n.*5081C>T
ENST00000696733.1:c.*3053C>T	ENSP00000512838.1:n.*3053C>T
ENST00000696734.1:c.*3086C>T	ENSP00000512839.1:n.*3086C>T
ENST00000696920.1:n.8694C>T
ENST00000696921.1:n.9537C>T
ENST00000696922.1:n.11362C>T
ENST00000696923.1:c.*3086C>T	ENSP00000512976.1:n.*3086C>T
ENST00000696924.1:c.*3053C>T	ENSP00000512977.1:n.*3053C>T
ENST00000343455.8:c.*2662C>T MANE Select	ENSP00000343745.3:n.*2662C>T
ENST00000526495.6:c.*2662C>T	ENSP00000437256.1:n.*2662C>T
ENST00000675540.1:c.6176C>T	ENSP00000501988.1:n.6176C>T
ENST00000343455.7:c.*2662C>T	ENSP00000343745.3:n.*2662C>T
ENST00000393063.5:c.*2662C>T	ENSP00000376783.1:n.*2662C>T
ENST00000526495.5:c.*2662C>T	ENSP00000437256.1:n.*2662C>T
NM_001195573.1:c.*2778C>T	NP_001182502.1:n.*2778C>T
NM_001271282.2:c.*2662C>T	NP_001258211.1:n.*2662C>T
NM_001291628.1:c.*2662C>T	NP_001278557.1:n.*2662C>T
NM_030621.4:c.*2662C>T	NP_085124.2:n.*2662C>T
NM_177438.2:c.*2662C>T , LRG_492t1:c.*2662C>T	NP_803187.1:n.*2662C>T
XM_011536599.1:c.*2662C>T	XP_011534901.1:n.*2662C>T
XM_011536600.1:c.*2662C>T	XP_011534902.1:n.*2662C>T
XM_011536601.1:c.*2662C>T	XP_011534903.1:n.*2662C>T
XM_011536602.1:c.*2662C>T	XP_011534904.1:n.*2662C>T
XM_011536603.1:c.*2662C>T	XP_011534905.1:n.*2662C>T
XM_011536604.1:c.*2662C>T	XP_011534906.1:n.*2662C>T
XM_011536605.1:c.*2662C>T	XP_011534907.1:n.*2662C>T
XM_011536599.2:c.*2662C>T	XP_011534901.1:n.*2662C>T
XM_011536600.3:c.*2662C>T	XP_011534902.1:n.*2662C>T
XM_011536601.3:c.*2662C>T	XP_011534903.1:n.*2662C>T
XM_011536602.3:c.*2662C>T	XP_011534904.1:n.*2662C>T
XM_011536604.2:c.*2662C>T	XP_011534906.1:n.*2662C>T
XM_011536605.2:c.*2662C>T	XP_011534907.1:n.*2662C>T
XM_017021120.2:c.*2662C>T	XP_016876609.1:n.*2662C>T
XM_017021121.2:c.*2662C>T	XP_016876610.1:n.*2662C>T
XM_017021122.2:c.*2662C>T	XP_016876611.1:n.*2662C>T
XM_017021123.2:c.*2662C>T	XP_016876612.1:n.*2662C>T
NM_001271282.3:c.*2662C>T	NP_001258211.1:n.*2662C>T
NM_001291628.2:c.*2662C>T	NP_001278557.1:n.*2662C>T
NM_177438.3:c.*2662C>T MANE Select	NP_803187.1:n.*2662C>T
NM_001395677.1:c.*2662C>T	NP_001382606.1:n.*2662C>T
NM_001395678.1:c.*2662C>T	NP_001382607.1:n.*2662C>T
NM_001395679.1:c.*2662C>T	NP_001382608.1:n.*2662C>T
NM_001395680.1:c.*2662C>T	NP_001382609.1:n.*2662C>T
NM_001395682.1:c.*2662C>T	NP_001382611.1:n.*2662C>T
NM_001395683.1:c.*2662C>T	NP_001382612.1:n.*2662C>T
NM_001395684.1:c.*2662C>T	NP_001382613.1:n.*2662C>T
NM_001395685.1:c.*2977C>T	NP_001382614.1:n.*2977C>T
NM_001395686.1:c.*2662C>T	NP_001382615.1:n.*2662C>T
NM_001395687.1:c.*2662C>T	NP_001382616.1:n.*2662C>T
NM_001395688.1:c.*2662C>T	NP_001382617.1:n.*2662C>T
NM_001395689.1:c.*2662C>T	NP_001382618.1:n.*2662C>T
NM_001395690.1:c.*2662C>T	NP_001382619.1:n.*2662C>T
NM_001395691.1:c.*2662C>T	NP_001382620.1:n.*2662C>T
NM_001395697.1:c.*2662C>T	NP_001382626.1:n.*2662C>T
NR_172715.1:n.6333-607C>T
NR_172716.1:n.9033C>T
NR_172717.1:n.6427-607C>T
NR_172718.1:n.8866C>T
NR_172719.1:n.8699C>T
NR_172720.1:n.8902C>T