Canonical Allele Identifier: CA2317589912
Gene: STK11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1220629_1220630delinsTC , CM000681.2:g.1220629_1220630delinsTC GRCh38
NC_000019.9:g.1220628_1220629delinsTC , CM000681.1:g.1220628_1220629delinsTC GRCh37
NC_000019.8:g.1171628_1171629delinsTC NCBI36
NG_007460.2:g.36223_36224delinsTC , LRG_319:g.36223_36224delinsTC

Transcript Alleles

HGVS Amino-acid change
ENST00000585465.3:c.646_647delinsTC ENSP00000490268.2:p.Ser216=
ENST00000585748.3:c.274_275delinsTC ENSP00000477641.2:p.Ser92=
ENST00000585851.2:c.472_473delinsTC ENSP00000467912.2:p.Ser158=
ENST00000326873.12:c.646_647delinsTC MANE Select ENSP00000324856.6:p.Ser216=
ENST00000652231.1:c.646_647delinsTC ENSP00000498804.1:p.Ser216=
ENST00000326873.11:c.646_647delinsTC ENSP00000324856.6:p.Ser216=
ENST00000586243.5:c.646_647delinsTC ENSP00000467240.2:p.Ser216=
ENST00000586358.5:n.544_545delinsTC
ENST00000589152.5:n.736_737delinsTC
ENST00000591133.2:n.617_618delinsTC
NM_000455.4:c.646_647delinsTC , LRG_319t1:c.646_647delinsTC NP_000446.1:p.Ser216=
XM_005259617.1:c.646_647delinsTC XP_005259674.1:p.Ser216=
XM_005259618.3:c.646_647delinsTC XP_005259675.1:p.Ser216=
XM_011528209.1:c.424_425delinsTC XP_011526511.1:p.Ser142=
XR_936204.1:n.1271_1272delinsTC
XM_005259617.3:c.646_647delinsTC XP_005259674.1:p.Ser216=
XM_011528209.2:c.424_425delinsTC XP_011526511.1:p.Ser142=
XR_001753738.2:n.1271_1272delinsTC
XR_001753739.1:n.1271_1272delinsTC
XR_001753740.2:n.1271_1272delinsTC
NM_000455.5:c.646_647delinsTC MANE Select NP_000446.1:p.Ser216=