Canonical Allele Identifier: CA645369766
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 428772
ClinVar RCV Id: RCV000492429
dbSNP Id: rs1131690936
MyVariant Identifiers: chr19:g.1207107_1207110del (hg19) chr19:g.1207108_1207111del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1207108_1207111del , CM000681.2:g.1207108_1207111del GRCh38
NC_000019.9:g.1207107_1207110del , CM000681.1:g.1207107_1207110del GRCh37
NC_000019.8:g.1158107_1158110del NCBI36
NG_007460.2:g.22702_22705del , LRG_319:g.22702_22705del

Transcript Alleles

HGVS Amino-acid change
ENST00000585465.3:c.195_198del ENSP00000490268.2:p.Glu65AspfsTer30
ENST00000585748.3:c.-82-11309_-82-11306del ENSP00000477641.2:n.-82-11309_-82-11306de...
ENST00000585851.2:c.195_198del ENSP00000467912.2:p.Glu65AspfsTer30
ENST00000326873.12:c.195_198del MANE Select ENSP00000324856.6:p.Glu65AspfsTer30
ENST00000652231.1:c.195_198del ENSP00000498804.1:p.Glu65AspfsTer30
ENST00000326873.11:c.195_198del ENSP00000324856.6:p.Glu65AspfsTer30
ENST00000585748.2:c.-82-11309_-82-11306del ENSP00000477641.1:n.-82-11309_-82-11306de...
ENST00000585851.1:c.195_198del ENSP00000467912.1:p.Glu65AspfsTer30
ENST00000586243.5:c.195_198del ENSP00000467240.2:p.Glu65AspfsTer30
ENST00000586358.5:n.18_21del
ENST00000589152.5:n.285_288del
ENST00000593219.5:c.195_198del ENSP00000466610.1:p.Glu65AspfsTer30
NM_000455.4:c.195_198del , LRG_319t1:c.195_198del NP_000446.1:p.Glu65AspfsTer30
XM_005259617.1:c.195_198del XP_005259674.1:p.Glu65AspfsTer30
XM_005259618.3:c.195_198del XP_005259675.1:p.Glu65AspfsTer30
XM_011528209.1:c.-159_-156del XP_011526511.1:n.-159_-156del
XR_936204.1:n.820_823del
XM_005259617.3:c.195_198del XP_005259674.1:p.Glu65AspfsTer30
XM_011528209.2:c.-159_-156del XP_011526511.1:n.-159_-156del
XR_001753738.2:n.820_823del
XR_001753739.1:n.820_823del
XR_001753740.2:n.820_823del
NM_000455.5:c.195_198del MANE Select NP_000446.1:p.Glu65AspfsTer30
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