Canonical Allele Identifier: CA2580613755

Gene: DICER1

Linked Data

• ClinVar Variation Id: 2503520
• ClinVar RCV Id: RCV003230335

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.95106964_95113363del , CM000676.2:g.95106964_95113363del	GRCh38
NC_000014.8:g.95573301_95579700del , CM000676.1:g.95573301_95579700del	GRCh37
NC_000014.7:g.94643054_94649453del	NCBI36
NG_016311.1:g.49061_55460del , LRG_492:g.49061_55460del

Transcript Alleles

HGVS	Amino-acid change
ENST00000529720.2:c.1908-138_2804+645del
ENST00000531162.7:c.1908-138_2804+645del
ENST00000674628.2:c.1908-138_2804+645del
ENST00000675540.2:c.1908-138_2804+645del
ENST00000696733.1:c.1908-138_2804+645del
ENST00000696734.1:c.1908-138_2804+645del
ENST00000696736.1:c.1908-138_2804+645del
ENST00000696737.1:c.1908-138_2804+645del
ENST00000696920.1:n.2171-138_3067+645del
ENST00000696921.1:n.3014-138_3910+645del
ENST00000696922.1:n.2317-138_3213+645del
ENST00000696923.1:c.1908-138_2804+645del
ENST00000696924.1:c.1908-138_2804+645del
ENST00000696925.1:n.2317-138_3213+645del
ENST00000343455.8:c.1908-138_2804+645del
ENST00000393063.6:c.1908-138_2804+645del
ENST00000526495.6:c.1908-138_2804+645del
ENST00000532939.3:c.1908-138_2804+645del
ENST00000556045.6:c.1908-138_2804+645del
ENST00000675995.1:c.*224-138_*1120+645del
ENST00000343455.7:c.1908-138_2804+645del
ENST00000393063.5:c.1908-138_2804+645del
ENST00000526495.5:c.1908-138_2804+645del
ENST00000527414.5:c.1908-138_2804+645del
ENST00000541352.5:c.1908-138_2804+645del
NM_001195573.1:c.1908-138_2804+645del
NM_001271282.2:c.1908-138_2804+645del
NM_001291628.1:c.1908-138_2804+645del
NM_030621.4:c.1908-138_2804+645del
NM_177438.2:c.1908-138_2804+645del , LRG_492t1:c.1908-138_2804+645del
XM_011536599.1:c.1908-138_2804+645del
XM_011536600.1:c.1908-138_2804+645del
XM_011536601.1:c.1908-138_2804+645del
XM_011536602.1:c.1908-138_2804+645del
XM_011536603.1:c.1908-138_2804+645del
XM_011536604.1:c.1503-138_2399+645del
XM_011536605.1:c.429-138_1325+645del
XM_011536599.2:c.1908-138_2804+645del
XM_011536600.3:c.1908-138_2804+645del
XM_011536601.3:c.1908-138_2804+645del
XM_011536602.3:c.1908-138_2804+645del
XM_011536604.2:c.1503-138_2399+645del
XM_011536605.2:c.429-138_1325+645del
XM_017021120.2:c.1908-138_2804+645del
XM_017021121.2:c.1908-138_2804+645del
XM_017021122.2:c.1503-138_2399+645del
XM_017021123.2:c.1503-138_2399+645del
NM_001271282.3:c.1908-138_2804+645del
NM_001291628.2:c.1908-138_2804+645del
NM_177438.3:c.1908-138_2804+645del
NM_001395677.1:c.1908-138_2804+645del
NM_001395678.1:c.1908-138_2804+645del
NM_001395679.1:c.1908-138_2804+645del
NM_001395680.1:c.1908-138_2804+645del
NM_001395682.1:c.1908-138_2804+645del
NM_001395683.1:c.1908-138_2804+645del
NM_001395684.1:c.1908-138_2804+645del
NM_001395685.1:c.1908-138_2804+645del
NM_001395686.1:c.1626-138_2522+645del
NM_001395687.1:c.1503-138_2399+645del
NM_001395688.1:c.1503-138_2399+645del
NM_001395689.1:c.1503-138_2399+645del
NM_001395690.1:c.1503-138_2399+645del
NM_001395691.1:c.1341-138_2237+645del
NM_001395692.1:c.1908-138_2804+645del
NM_001395693.1:c.1908-138_2804+645del
NM_001395694.1:c.1908-138_2804+645del
NM_001395695.1:c.1908-138_2804+645del
NM_001395696.1:c.1503-138_2399+645del
NM_001395697.1:c.225-138_1121+645del
NR_172715.1:n.2326-138_3222+645del
NR_172716.1:n.2253-138_3149+645del
NR_172717.1:n.2420-138_3316+645del
NR_172718.1:n.2420-138_3316+645del
NR_172719.1:n.2253-138_3149+645del
NR_172720.1:n.2253-138_3149+645del