Canonical Allele Identifier: CA645369775
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 428793
ClinVar RCV Id: RCV000492760 RCV000583353 RCV002523987
dbSNP Id: rs1131690953
MyVariant Identifiers: chr19:g.1207071_1207082del (hg19) chr19:g.1207072_1207083del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1207072_1207083del , CM000681.2:g.1207072_1207083del GRCh38
NC_000019.9:g.1207071_1207082del , CM000681.1:g.1207071_1207082del GRCh37
NC_000019.8:g.1158071_1158082del NCBI36
NG_007460.2:g.22666_22677del , LRG_319:g.22666_22677del

Transcript Alleles

HGVS Amino-acid change
ENST00000585465.3:c.159_170del ENSP00000490268.2:p.Asp53_Gly56del
ENST00000585748.3:c.-82-11345_-82-11334del ENSP00000477641.2:n.-82-11345_-82-11334de...
ENST00000585851.2:c.159_170del ENSP00000467912.2:p.Asp53_Gly56del
ENST00000326873.12:c.159_170del MANE Select ENSP00000324856.6:p.Asp53_Gly56del
ENST00000652231.1:c.159_170del ENSP00000498804.1:p.Asp53_Gly56del
ENST00000326873.11:c.159_170del ENSP00000324856.6:p.Asp53_Gly56del
ENST00000585748.2:c.-82-11345_-82-11334del ENSP00000477641.1:n.-82-11345_-82-11334de...
ENST00000585851.1:c.159_170del ENSP00000467912.1:p.Asp53_Gly56del
ENST00000586243.5:c.159_170del ENSP00000467240.2:p.Asp53_Gly56del
ENST00000589152.5:n.249_260del
ENST00000593219.5:c.159_170del ENSP00000466610.1:p.Asp53_Gly56del
NM_000455.4:c.159_170del , LRG_319t1:c.159_170del NP_000446.1:p.Asp53_Gly56del
XM_005259617.1:c.159_170del XP_005259674.1:p.Asp53_Gly56del
XM_005259618.3:c.159_170del XP_005259675.1:p.Asp53_Gly56del
XM_011528209.1:c.-195_-184del XP_011526511.1:n.-195_-184del
XR_936204.1:n.784_795del
XM_005259617.3:c.159_170del XP_005259674.1:p.Asp53_Gly56del
XM_011528209.2:c.-195_-184del XP_011526511.1:n.-195_-184del
XR_001753738.2:n.784_795del
XR_001753739.1:n.784_795del
XR_001753740.2:n.784_795del
NM_000455.5:c.159_170del MANE Select NP_000446.1:p.Asp53_Gly56del
Search 100 bp 5'
Search 100 bp 3'