Canonical Allele Identifier: CA2317589694
Gene: STK11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1220320_1220322delinsCCT , CM000681.2:g.1220320_1220322delinsCCT GRCh38
NC_000019.9:g.1220319_1220321delinsCCT , CM000681.1:g.1220319_1220321delinsCCT GRCh37
NC_000019.8:g.1171319_1171321delinsCCT NCBI36
NG_007460.2:g.35914_35916delinsCCT , LRG_319:g.35914_35916delinsCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.465-53_465-51delinsCCT ENSP00000490268.2:n.465-53_465-51delinsCCT
ENST00000585748.3:c.93-53_93-51delinsCCT ENSP00000477641.2:n.93-53_93-51delinsCCT
ENST00000585851.2:c.291-53_291-51delinsCCT ENSP00000467912.2:n.291-53_291-51delinsCCT
ENST00000326873.12:c.465-53_465-51delinsCCT MANE Select ENSP00000324856.6:n.465-53_465-51delinsCCT
ENST00000652231.1:c.465-53_465-51delinsCCT ENSP00000498804.1:n.465-53_465-51delinsCCT
ENST00000326873.11:c.465-53_465-51delinsCCT ENSP00000324856.6:n.465-53_465-51delinsCCT
ENST00000585851.1:c.291-53_291-51delinsCCT ENSP00000467912.1:n.291-53_291-51delinsCCT
ENST00000586243.5:c.465-53_465-51delinsCCT ENSP00000467240.2:n.465-53_465-51delinsCCT
ENST00000586358.5:n.288-53_288-51delinsCCT
ENST00000589152.5:n.555-53_555-51delinsCCT
ENST00000591133.2:n.308_310delinsCCT
NM_000455.4:c.465-53_465-51delinsCCT , LRG_319t1:c.465-53_465-51delinsCCT NP_000446.1:n.465-53_465-51delinsCCT
XM_005259617.1:c.465-53_465-51delinsCCT XP_005259674.1:n.465-53_465-51delinsCCT
XM_005259618.3:c.465-53_465-51delinsCCT XP_005259675.1:n.465-53_465-51delinsCCT
XM_011528209.1:c.243-53_243-51delinsCCT XP_011526511.1:n.243-53_243-51delinsCCT
XR_936204.1:n.1090-53_1090-51delinsCCT
XM_005259617.3:c.465-53_465-51delinsCCT XP_005259674.1:n.465-53_465-51delinsCCT
XM_011528209.2:c.243-53_243-51delinsCCT XP_011526511.1:n.243-53_243-51delinsCCT
XR_001753738.2:n.1090-53_1090-51delinsCCT
XR_001753739.1:n.1090-53_1090-51delinsCCT
XR_001753740.2:n.1090-53_1090-51delinsCCT
NM_000455.5:c.465-53_465-51delinsCCT MANE Select NP_000446.1:n.465-53_465-51delinsCCT