Canonical Allele Identifier: CA645369738
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 428762
ClinVar RCV Id: RCV000492754
dbSNP Id: rs1131690926
MyVariant Identifiers: chr19:g.1219394del (hg19) chr19:g.1219395del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1219395del , CM000681.2:g.1219395del GRCh38
NC_000019.9:g.1219394del , CM000681.1:g.1219394del GRCh37
NC_000019.8:g.1170394del NCBI36
NG_007460.2:g.34989del , LRG_319:g.34989del

Transcript Alleles

HGVS Amino-acid change
ENST00000585465.3:c.446del ENSP00000490268.2:p.Pro149GlnfsTer12
ENST00000585748.3:c.74del ENSP00000477641.2:p.Pro25GlnfsTer12
ENST00000585851.2:c.291-978del ENSP00000467912.2:n.291-978del
ENST00000326873.12:c.446del MANE Select ENSP00000324856.6:p.Pro149GlnfsTer12
ENST00000652231.1:c.446del ENSP00000498804.1:p.Pro149GlnfsTer12
ENST00000326873.11:c.446del ENSP00000324856.6:p.Pro149GlnfsTer12
ENST00000585851.1:c.291-978del ENSP00000467912.1:n.291-978del
ENST00000586243.5:c.446del ENSP00000467240.2:p.Pro149GlnfsTer12
ENST00000586358.5:n.269del
ENST00000589152.5:n.536del
NM_000455.4:c.446del , LRG_319t1:c.446del NP_000446.1:p.Pro149GlnfsTer12
XM_005259617.1:c.446del XP_005259674.1:p.Pro149GlnfsTer12
XM_005259618.3:c.446del XP_005259675.1:p.Pro149GlnfsTer12
XM_011528209.1:c.224del XP_011526511.1:p.Pro75GlnfsTer12
XR_936204.1:n.1071del
XM_005259617.3:c.446del XP_005259674.1:p.Pro149GlnfsTer12
XM_011528209.2:c.224del XP_011526511.1:p.Pro75GlnfsTer12
XR_001753738.2:n.1071del
XR_001753739.1:n.1071del
XR_001753740.2:n.1071del
NM_000455.5:c.446del MANE Select NP_000446.1:p.Pro149GlnfsTer12
Search 100 bp 5'
Search 100 bp 3'