Canonical Allele Identifier: CA2317589131
Gene: STK11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1219420_1219421delinsGC , CM000681.2:g.1219420_1219421delinsGC GRCh38
NC_000019.9:g.1219419_1219420delinsGC , CM000681.1:g.1219419_1219420delinsGC GRCh37
NC_000019.8:g.1170419_1170420delinsGC NCBI36
NG_007460.2:g.35014_35015delinsGC , LRG_319:g.35014_35015delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.464+7_464+8delinsGC ENSP00000490268.2:n.464+7_464+8delinsGC
ENST00000585748.3:c.92+7_92+8delinsGC ENSP00000477641.2:n.92+7_92+8delinsGC
ENST00000585851.2:c.291-953_291-952delinsGC ENSP00000467912.2:n.291-953_291-952delinsGC
ENST00000326873.12:c.464+7_464+8delinsGC MANE Select ENSP00000324856.6:n.464+7_464+8delinsGC
ENST00000652231.1:c.464+7_464+8delinsGC ENSP00000498804.1:n.464+7_464+8delinsGC
ENST00000326873.11:c.464+7_464+8delinsGC ENSP00000324856.6:n.464+7_464+8delinsGC
ENST00000585851.1:c.291-953_291-952delinsGC ENSP00000467912.1:n.291-953_291-952delinsGC
ENST00000586243.5:c.464+7_464+8delinsGC ENSP00000467240.2:n.464+7_464+8delinsGC
ENST00000586358.5:n.287+7_287+8delinsGC
ENST00000589152.5:n.554+7_554+8delinsGC
NM_000455.4:c.464+7_464+8delinsGC , LRG_319t1:c.464+7_464+8delinsGC NP_000446.1:n.464+7_464+8delinsGC
XM_005259617.1:c.464+7_464+8delinsGC XP_005259674.1:n.464+7_464+8delinsGC
XM_005259618.3:c.464+7_464+8delinsGC XP_005259675.1:n.464+7_464+8delinsGC
XM_011528209.1:c.242+7_242+8delinsGC XP_011526511.1:n.242+7_242+8delinsGC
XR_936204.1:n.1089+7_1089+8delinsGC
XM_005259617.3:c.464+7_464+8delinsGC XP_005259674.1:n.464+7_464+8delinsGC
XM_011528209.2:c.242+7_242+8delinsGC XP_011526511.1:n.242+7_242+8delinsGC
XR_001753738.2:n.1089+7_1089+8delinsGC
XR_001753739.1:n.1089+7_1089+8delinsGC
XR_001753740.2:n.1089+7_1089+8delinsGC
NM_000455.5:c.464+7_464+8delinsGC MANE Select NP_000446.1:n.464+7_464+8delinsGC