Canonical Allele Identifier: CA10646649

Gene: DICER1

Linked Data

• ClinVar Variation Id: 315053
• ClinVar RCV Id: RCV000334079
• dbSNP Id: rs180705469
• gnomAD v2: 14-95553523-C-A
• gnomAD v3: 14-95087186-C-A
• gnomAD v4: 14-95087186-C-A
• MyVariant Identifiers: chr14:g.95553523C>A (hg19) ; chr14:g.95087186C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.95087186C>A , CM000676.2:g.95087186C>A	GRCh38
NC_000014.8:g.95553523C>A , CM000676.1:g.95553523C>A	GRCh37
NC_000014.7:g.94623276C>A	NCBI36
NG_016311.1:g.75237G>T , LRG_492:g.75237G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000529720.2:c.*3312G>T	ENSP00000433926.2:n.*3312G>T
ENST00000531162.7:c.*3312G>T	ENSP00000433060.3:n.*3312G>T
ENST00000674628.2:c.*3312G>T	ENSP00000502730.2:n.*3312G>T
ENST00000675540.2:c.*5731G>T	ENSP00000501988.2:n.*5731G>T
ENST00000696733.1:c.*3703G>T	ENSP00000512838.1:n.*3703G>T
ENST00000696734.1:c.*3736G>T	ENSP00000512839.1:n.*3736G>T
ENST00000696920.1:n.9344G>T
ENST00000696921.1:n.10187G>T
ENST00000696922.1:n.12012G>T
ENST00000696923.1:c.*3736G>T	ENSP00000512976.1:n.*3736G>T
ENST00000696924.1:c.*3703G>T	ENSP00000512977.1:n.*3703G>T
ENST00000343455.8:c.*3312G>T MANE Select	ENSP00000343745.3:n.*3312G>T
ENST00000526495.6:c.*3312G>T	ENSP00000437256.1:n.*3312G>T
ENST00000675540.1:c.6826G>T	ENSP00000501988.1:n.6826G>T
ENST00000343455.7:c.*3312G>T	ENSP00000343745.3:n.*3312G>T
ENST00000393063.5:c.*3312G>T	ENSP00000376783.1:n.*3312G>T
ENST00000526495.5:c.*3312G>T	ENSP00000437256.1:n.*3312G>T
NM_001195573.1:c.*3428G>T	NP_001182502.1:n.*3428G>T
NM_001271282.2:c.*3312G>T	NP_001258211.1:n.*3312G>T
NM_001291628.1:c.*3312G>T	NP_001278557.1:n.*3312G>T
NM_030621.4:c.*3312G>T	NP_085124.2:n.*3312G>T
NM_177438.2:c.*3312G>T , LRG_492t1:c.*3312G>T	NP_803187.1:n.*3312G>T
XM_011536599.1:c.*3312G>T	XP_011534901.1:n.*3312G>T
XM_011536600.1:c.*3312G>T	XP_011534902.1:n.*3312G>T
XM_011536601.1:c.*3312G>T	XP_011534903.1:n.*3312G>T
XM_011536602.1:c.*3312G>T	XP_011534904.1:n.*3312G>T
XM_011536603.1:c.*3312G>T	XP_011534905.1:n.*3312G>T
XM_011536604.1:c.*3312G>T	XP_011534906.1:n.*3312G>T
XM_011536605.1:c.*3312G>T	XP_011534907.1:n.*3312G>T
XM_011536599.2:c.*3312G>T	XP_011534901.1:n.*3312G>T
XM_011536600.3:c.*3312G>T	XP_011534902.1:n.*3312G>T
XM_011536601.3:c.*3312G>T	XP_011534903.1:n.*3312G>T
XM_011536602.3:c.*3312G>T	XP_011534904.1:n.*3312G>T
XM_011536604.2:c.*3312G>T	XP_011534906.1:n.*3312G>T
XM_011536605.2:c.*3312G>T	XP_011534907.1:n.*3312G>T
XM_017021120.2:c.*3312G>T	XP_016876609.1:n.*3312G>T
XM_017021121.2:c.*3312G>T	XP_016876610.1:n.*3312G>T
XM_017021122.2:c.*3312G>T	XP_016876611.1:n.*3312G>T
XM_017021123.2:c.*3312G>T	XP_016876612.1:n.*3312G>T
NM_001271282.3:c.*3312G>T	NP_001258211.1:n.*3312G>T
NM_001291628.2:c.*3312G>T	NP_001278557.1:n.*3312G>T
NM_177438.3:c.*3312G>T MANE Select	NP_803187.1:n.*3312G>T
NM_001395677.1:c.*3312G>T	NP_001382606.1:n.*3312G>T
NM_001395678.1:c.*3312G>T	NP_001382607.1:n.*3312G>T
NM_001395679.1:c.*3312G>T	NP_001382608.1:n.*3312G>T
NM_001395680.1:c.*3312G>T	NP_001382609.1:n.*3312G>T
NM_001395682.1:c.*3312G>T	NP_001382611.1:n.*3312G>T
NM_001395683.1:c.*3312G>T	NP_001382612.1:n.*3312G>T
NM_001395684.1:c.*3312G>T	NP_001382613.1:n.*3312G>T
NM_001395685.1:c.*3627G>T	NP_001382614.1:n.*3627G>T
NM_001395686.1:c.*3312G>T	NP_001382615.1:n.*3312G>T
NM_001395687.1:c.*3312G>T	NP_001382616.1:n.*3312G>T
NM_001395688.1:c.*3312G>T	NP_001382617.1:n.*3312G>T
NM_001395689.1:c.*3312G>T	NP_001382618.1:n.*3312G>T
NM_001395690.1:c.*3312G>T	NP_001382619.1:n.*3312G>T
NM_001395691.1:c.*3312G>T	NP_001382620.1:n.*3312G>T
NM_001395697.1:c.*3312G>T	NP_001382626.1:n.*3312G>T
NR_172715.1:n.6376G>T
NR_172716.1:n.9683G>T
NR_172717.1:n.6470G>T
NR_172718.1:n.9516G>T
NR_172719.1:n.9349G>T
NR_172720.1:n.9552G>T