Canonical Allele Identifier: CA023342
Gene: STK11 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1221994_1222002del , CM000681.2:g.1221994_1222002del GRCh38
NC_000019.9:g.1221993_1222001del , CM000681.1:g.1221993_1222001del GRCh37
NC_000019.8:g.1172993_1173001del NCBI36
NG_007460.2:g.37588_37596del , LRG_319:g.37588_37596del

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.908_916del ENSP00000490268.2:p.Ile303_His306delinsAsn
ENST00000585748.3:c.536_544del ENSP00000477641.2:p.Ile179_His182delinsAsn
ENST00000585851.2:c.734_742del ENSP00000467912.2:p.Ile245_His248delinsAsn
ENST00000326873.12:c.908_916del MANE Select ENSP00000324856.6:p.Ile303_His306delinsAsn
ENST00000652231.1:c.908_916del ENSP00000498804.1:p.Ile303_His306delinsAsn
ENST00000326873.11:c.908_916del ENSP00000324856.6:p.Ile303_His306delinsAsn
ENST00000586243.5:c.908_916del ENSP00000467240.2:p.Ile303_His306delinsAsn
ENST00000589152.5:n.1606_1614del
ENST00000591133.2:n.879_887del
NM_000455.4:c.908_916del , LRG_319t1:c.908_916del NP_000446.1:p.Ile303_His306delinsAsn
XM_005259617.1:c.908_916del XP_005259674.1:p.Ile303_His306delinsAsn
XM_005259618.3:c.908_916del XP_005259675.1:p.Ile303_His306delinsAsn
XM_011528209.1:c.686_694del XP_011526511.1:p.Ile229_His232delinsAsn
XR_936204.1:n.1684_1692del
XM_005259617.3:c.908_916del XP_005259674.1:p.Ile303_His306delinsAsn
XM_011528209.2:c.686_694del XP_011526511.1:p.Ile229_His232delinsAsn
XR_001753738.2:n.1714_1722del
XR_001753739.1:n.1714_1722del
XR_001753740.2:n.1684_1692del
NM_000455.5:c.908_916del MANE Select NP_000446.1:p.Ile303_His306delinsAsn
Search 100 bp 5'
Search 100 bp 3'