Canonical Allele Identifier: CA2598388824

Gene: DICER1

Linked Data

• dbSNP Id: rs2139747398
• gnomAD v3: 14-95088087-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.95088087C>T , CM000676.2:g.95088087C>T	GRCh38
NC_000014.8:g.95554424C>T , CM000676.1:g.95554424C>T	GRCh37
NC_000014.7:g.94624177C>T	NCBI36
NG_016311.1:g.74336G>A , LRG_492:g.74336G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529720.2:c.*2411G>A	ENSP00000433926.2:n.*2411G>A
ENST00000531162.7:c.*2411G>A	ENSP00000433060.3:n.*2411G>A
ENST00000674628.2:c.*2411G>A	ENSP00000502730.2:n.*2411G>A
ENST00000675540.2:c.*4830G>A	ENSP00000501988.2:n.*4830G>A
ENST00000696733.1:c.*2802G>A	ENSP00000512838.1:n.*2802G>A
ENST00000696734.1:c.*2835G>A	ENSP00000512839.1:n.*2835G>A
ENST00000696920.1:n.8443G>A
ENST00000696921.1:n.9286G>A
ENST00000696922.1:n.11111G>A
ENST00000696923.1:c.*2835G>A	ENSP00000512976.1:n.*2835G>A
ENST00000696924.1:c.*2802G>A	ENSP00000512977.1:n.*2802G>A
ENST00000343455.8:c.*2411G>A MANE Select	ENSP00000343745.3:n.*2411G>A
ENST00000526495.6:c.*2411G>A	ENSP00000437256.1:n.*2411G>A
ENST00000675540.1:c.5925G>A	ENSP00000501988.1:n.5925G>A
ENST00000343455.7:c.*2411G>A	ENSP00000343745.3:n.*2411G>A
ENST00000393063.5:c.*2411G>A	ENSP00000376783.1:n.*2411G>A
ENST00000526495.5:c.*2411G>A	ENSP00000437256.1:n.*2411G>A
NM_001195573.1:c.*2527G>A	NP_001182502.1:n.*2527G>A
NM_001271282.2:c.*2411G>A	NP_001258211.1:n.*2411G>A
NM_001291628.1:c.*2411G>A	NP_001278557.1:n.*2411G>A
NM_030621.4:c.*2411G>A	NP_085124.2:n.*2411G>A
NM_177438.2:c.*2411G>A , LRG_492t1:c.*2411G>A	NP_803187.1:n.*2411G>A
XM_011536599.1:c.*2411G>A	XP_011534901.1:n.*2411G>A
XM_011536600.1:c.*2411G>A	XP_011534902.1:n.*2411G>A
XM_011536601.1:c.*2411G>A	XP_011534903.1:n.*2411G>A
XM_011536602.1:c.*2411G>A	XP_011534904.1:n.*2411G>A
XM_011536603.1:c.*2411G>A	XP_011534905.1:n.*2411G>A
XM_011536604.1:c.*2411G>A	XP_011534906.1:n.*2411G>A
XM_011536605.1:c.*2411G>A	XP_011534907.1:n.*2411G>A
XM_011536599.2:c.*2411G>A	XP_011534901.1:n.*2411G>A
XM_011536600.3:c.*2411G>A	XP_011534902.1:n.*2411G>A
XM_011536601.3:c.*2411G>A	XP_011534903.1:n.*2411G>A
XM_011536602.3:c.*2411G>A	XP_011534904.1:n.*2411G>A
XM_011536604.2:c.*2411G>A	XP_011534906.1:n.*2411G>A
XM_011536605.2:c.*2411G>A	XP_011534907.1:n.*2411G>A
XM_017021120.2:c.*2411G>A	XP_016876609.1:n.*2411G>A
XM_017021121.2:c.*2411G>A	XP_016876610.1:n.*2411G>A
XM_017021122.2:c.*2411G>A	XP_016876611.1:n.*2411G>A
XM_017021123.2:c.*2411G>A	XP_016876612.1:n.*2411G>A
NM_001271282.3:c.*2411G>A	NP_001258211.1:n.*2411G>A
NM_001291628.2:c.*2411G>A	NP_001278557.1:n.*2411G>A
NM_177438.3:c.*2411G>A MANE Select	NP_803187.1:n.*2411G>A
NM_001395677.1:c.*2411G>A	NP_001382606.1:n.*2411G>A
NM_001395678.1:c.*2411G>A	NP_001382607.1:n.*2411G>A
NM_001395679.1:c.*2411G>A	NP_001382608.1:n.*2411G>A
NM_001395680.1:c.*2411G>A	NP_001382609.1:n.*2411G>A
NM_001395682.1:c.*2411G>A	NP_001382611.1:n.*2411G>A
NM_001395683.1:c.*2411G>A	NP_001382612.1:n.*2411G>A
NM_001395684.1:c.*2411G>A	NP_001382613.1:n.*2411G>A
NM_001395685.1:c.*2726G>A	NP_001382614.1:n.*2726G>A
NM_001395686.1:c.*2411G>A	NP_001382615.1:n.*2411G>A
NM_001395687.1:c.*2411G>A	NP_001382616.1:n.*2411G>A
NM_001395688.1:c.*2411G>A	NP_001382617.1:n.*2411G>A
NM_001395689.1:c.*2411G>A	NP_001382618.1:n.*2411G>A
NM_001395690.1:c.*2411G>A	NP_001382619.1:n.*2411G>A
NM_001395691.1:c.*2411G>A	NP_001382620.1:n.*2411G>A
NM_001395697.1:c.*2411G>A	NP_001382626.1:n.*2411G>A
NR_172715.1:n.6332+762G>A
NR_172716.1:n.8782G>A
NR_172717.1:n.6426+762G>A
NR_172718.1:n.8615G>A
NR_172719.1:n.8448G>A
NR_172720.1:n.8651G>A