Canonical Allele Identifier: CA7331007
Gene: DICER1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 485526
ClinVar RCV Id: RCV000564197
dbSNP Id: rs184830847

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.95103721G>A , CM000676.2:g.95103721G>A GRCh38
NC_000014.8:g.95570058G>A , CM000676.1:g.95570058G>A GRCh37
NC_000014.7:g.94639811G>A NCBI36
NG_016311.1:g.58702C>T , LRG_492:g.58702C>T

Transcript Alleles

HGVS Amino-acid change
NM_001195573.1:c.3675C>T VV NP_001182502.1:p.Tyr1225=
NM_001271282.2:c.3675C>T VV NP_001258211.1:p.Tyr1225=
NM_001291628.1:c.3675C>T VV NP_001278557.1:p.Tyr1225=
NM_030621.4:c.3675C>T VV NP_085124.2:p.Tyr1225=
NM_177438.2:c.3675C>T , LRG_492t1:c.3675C>T NP_803187.1:p.Tyr1225=
XM_011536599.1:c.3675C>T XP_011534901.1:p.Tyr1225=
XM_011536600.1:c.3675C>T XP_011534902.1:p.Tyr1225=
XM_011536601.1:c.3675C>T XP_011534903.1:p.Tyr1225=
XM_011536602.1:c.3675C>T XP_011534904.1:p.Tyr1225=
XM_011536603.1:c.3675C>T XP_011534905.1:p.Tyr1225=
XM_011536604.1:c.3270C>T XP_011534906.1:p.Tyr1090=
XM_011536605.1:c.2196C>T XP_011534907.1:p.Tyr732=
XM_011536599.2:c.3675C>T XP_011534901.1:p.Tyr1225=
XM_011536600.3:c.3675C>T XP_011534902.1:p.Tyr1225=
XM_011536601.3:c.3675C>T XP_011534903.1:p.Tyr1225=
XM_011536602.3:c.3675C>T XP_011534904.1:p.Tyr1225=
XM_011536604.2:c.3270C>T XP_011534906.1:p.Tyr1090=
XM_011536605.2:c.2196C>T XP_011534907.1:p.Tyr732=
XM_017021120.2:c.3675C>T XP_016876609.1:p.Tyr1225=
XM_017021121.2:c.3675C>T XP_016876610.1:p.Tyr1225=
XM_017021122.2:c.3270C>T XP_016876611.1:p.Tyr1090=
XM_017021123.2:c.3270C>T XP_016876612.1:p.Tyr1090=
ENST00000343455.7:c.3675C>T ENSP00000343745.3:p.Tyr1225=
ENST00000393063.5:c.3675C>T ENSP00000376783.1:p.Tyr1225=
ENST00000526495.5:c.3675C>T ENSP00000437256.1:p.Tyr1225=
ENST00000527414.5:c.3675C>T ENSP00000435681.1:p.Tyr1225=
ENST00000541352.5:c.3675C>T ENSP00000444719.1:p.Tyr1225=
ENST00000554367.1:n.884C>T
ENST00000556045.5:c.369C>T ENSP00000451041.1:p.Tyr123=