Canonical Allele Identifier: CA2317591534
Gene: STK11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1223104_1223110delinsCGGACGA , CM000681.2:g.1223104_1223110delinsCGGACGA GRCh38
NC_000019.9:g.1223103_1223109delinsCGGACGA , CM000681.1:g.1223103_1223109delinsCGGACGA GRCh37
NC_000019.8:g.1174103_1174109delinsCGGACGA NCBI36
NG_007460.2:g.38698_38704delinsCGGACGA , LRG_319:g.38698_38704delinsCGGACGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.1040_1046delinsCGGACGA ENSP00000490268.2:p.Ala347=
ENST00000585748.3:c.668_674delinsCGGACGA ENSP00000477641.2:p.Ala223=
ENST00000585851.2:c.866_872delinsCGGACGA ENSP00000467912.2:p.Ala289=
ENST00000326873.12:c.1040_1046delinsCGGACGA MANE Select ENSP00000324856.6:p.Ala347=
ENST00000652231.1:c.1040_1046delinsCGGACGA ENSP00000498804.1:p.Ala347=
ENST00000326873.11:c.1040_1046delinsCGGACGA ENSP00000324856.6:p.Ala347=
ENST00000586243.5:c.1040_1046delinsCGGACGA ENSP00000467240.2:p.Ala347=
ENST00000589152.5:n.1738_1744delinsCGGACGA
NM_000455.4:c.1040_1046delinsCGGACGA , LRG_319t1:c.1040_1046delinsCGGACGA NP_000446.1:p.Ala347=
XM_005259617.1:c.1040_1046delinsCGGACGA XP_005259674.1:p.Ala347=
XM_005259618.3:c.1040_1046delinsCGGACGA XP_005259675.1:p.Ala347=
XM_011528209.1:c.818_824delinsCGGACGA XP_011526511.1:p.Ala273=
XR_936204.1:n.1816_1822delinsCGGACGA
XM_005259617.3:c.1040_1046delinsCGGACGA XP_005259674.1:p.Ala347=
XM_011528209.2:c.818_824delinsCGGACGA XP_011526511.1:p.Ala273=
XR_001753738.2:n.1846_1852delinsCGGACGA
XR_001753739.1:n.1846_1852delinsCGGACGA
XR_001753740.2:n.1816_1822delinsCGGACGA
NM_000455.5:c.1040_1046delinsCGGACGA MANE Select NP_000446.1:p.Ala347=