Canonical Allele Identifier: CA2580096085
Gene: STK11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1220635del , CM000681.2:g.1220635del GRCh38
NC_000019.9:g.1220634del , CM000681.1:g.1220634del GRCh37
NC_000019.8:g.1171634del NCBI36
NG_007460.2:g.36229del , LRG_319:g.36229del

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.652del ENSP00000490268.2:p.Ala218LeufsTer?
ENST00000585748.3:c.280del ENSP00000477641.2:p.Ala94LeufsTer?
ENST00000585851.2:c.478del ENSP00000467912.2:p.Ala160LeufsTer?
ENST00000326873.12:c.652del MANE Select ENSP00000324856.6:p.Ala218LeufsTer?
ENST00000652231.1:c.652del ENSP00000498804.1:p.Ala218LeufsTer?
ENST00000326873.11:c.652del ENSP00000324856.6:p.Ala218LeufsTer?
ENST00000586243.5:c.652del ENSP00000467240.2:p.Ala218LeufsTer?
ENST00000586358.5:n.550del
ENST00000589152.5:n.742del
ENST00000591133.2:n.623del
NM_000455.4:c.652del , LRG_319t1:c.652del NP_000446.1:p.Ala218LeufsTer?
XM_005259617.1:c.652del XP_005259674.1:p.Ala218LeufsTer?
XM_005259618.3:c.652del XP_005259675.1:p.Ala218LeufsTer?
XM_011528209.1:c.430del XP_011526511.1:p.Ala144LeufsTer?
XR_936204.1:n.1277del
XM_005259617.3:c.652del XP_005259674.1:p.Ala218LeufsTer?
XM_011528209.2:c.430del XP_011526511.1:p.Ala144LeufsTer?
XR_001753738.2:n.1277del
XR_001753739.1:n.1277del
XR_001753740.2:n.1277del
NM_000455.5:c.652del MANE Select NP_000446.1:p.Ala218LeufsTer?