Canonical Allele Identifier: CA2317589683
Gene: STK11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1220306_1220307delinsCT , CM000681.2:g.1220306_1220307delinsCT GRCh38
NC_000019.9:g.1220305_1220306delinsCT , CM000681.1:g.1220305_1220306delinsCT GRCh37
NC_000019.8:g.1171305_1171306delinsCT NCBI36
NG_007460.2:g.35900_35901delinsCT , LRG_319:g.35900_35901delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.465-67_465-66delinsCT ENSP00000490268.2:n.465-67_465-66delinsCT
ENST00000585748.3:c.93-67_93-66delinsCT ENSP00000477641.2:n.93-67_93-66delinsCT
ENST00000585851.2:c.291-67_291-66delinsCT ENSP00000467912.2:n.291-67_291-66delinsCT
ENST00000326873.12:c.465-67_465-66delinsCT MANE Select ENSP00000324856.6:n.465-67_465-66delinsCT
ENST00000652231.1:c.465-67_465-66delinsCT ENSP00000498804.1:n.465-67_465-66delinsCT
ENST00000326873.11:c.465-67_465-66delinsCT ENSP00000324856.6:n.465-67_465-66delinsCT
ENST00000585851.1:c.291-67_291-66delinsCT ENSP00000467912.1:n.291-67_291-66delinsCT
ENST00000586243.5:c.465-67_465-66delinsCT ENSP00000467240.2:n.465-67_465-66delinsCT
ENST00000586358.5:n.288-67_288-66delinsCT
ENST00000589152.5:n.555-67_555-66delinsCT
ENST00000591133.2:n.294_295delinsCT
NM_000455.4:c.465-67_465-66delinsCT , LRG_319t1:c.465-67_465-66delinsCT NP_000446.1:n.465-67_465-66delinsCT
XM_005259617.1:c.465-67_465-66delinsCT XP_005259674.1:n.465-67_465-66delinsCT
XM_005259618.3:c.465-67_465-66delinsCT XP_005259675.1:n.465-67_465-66delinsCT
XM_011528209.1:c.243-67_243-66delinsCT XP_011526511.1:n.243-67_243-66delinsCT
XR_936204.1:n.1090-67_1090-66delinsCT
XM_005259617.3:c.465-67_465-66delinsCT XP_005259674.1:n.465-67_465-66delinsCT
XM_011528209.2:c.243-67_243-66delinsCT XP_011526511.1:n.243-67_243-66delinsCT
XR_001753738.2:n.1090-67_1090-66delinsCT
XR_001753739.1:n.1090-67_1090-66delinsCT
XR_001753740.2:n.1090-67_1090-66delinsCT
NM_000455.5:c.465-67_465-66delinsCT MANE Select NP_000446.1:n.465-67_465-66delinsCT