Canonical Allele Identifier: CA2317589058
Gene: STK11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1219324G= , CM000681.2:g.1219324G= GRCh38
NC_000019.9:g.1219323G= , CM000681.1:g.1219323G= GRCh37
NC_000019.8:g.1170323G= NCBI36
NG_007460.2:g.34918G= , LRG_319:g.34918G=

Transcript Alleles

HGVS Amino-acid change
ENST00000585465.3:c.375G= ENSP00000490268.2:p.Met125=
ENST00000585748.3:c.3G= ENSP00000477641.2:p.Met1=
ENST00000585851.2:c.291-1049G= ENSP00000467912.2:n.291-1049G=
ENST00000326873.12:c.375G= MANE Select ENSP00000324856.6:p.Met125=
ENST00000652231.1:c.375G= ENSP00000498804.1:p.Met125=
ENST00000326873.11:c.375G= ENSP00000324856.6:p.Met125=
ENST00000585748.2:c.3G= ENSP00000477641.1:p.Met1=
ENST00000585851.1:c.291-1049G= ENSP00000467912.1:n.291-1049G=
ENST00000586243.5:c.375G= ENSP00000467240.2:p.Met125=
ENST00000586358.5:n.198G=
ENST00000589152.5:n.465G=
ENST00000593219.5:c.*200G= ENSP00000466610.1:n.*200G=
NM_000455.4:c.375G= , LRG_319t1:c.375G= NP_000446.1:p.Met125=
XM_005259617.1:c.375G= XP_005259674.1:p.Met125=
XM_005259618.3:c.375G= XP_005259675.1:p.Met125=
XM_011528209.1:c.153G= XP_011526511.1:p.Met51=
XR_936204.1:n.1000G=
XM_005259617.3:c.375G= XP_005259674.1:p.Met125=
XM_011528209.2:c.153G= XP_011526511.1:p.Met51=
XR_001753738.2:n.1000G=
XR_001753739.1:n.1000G=
XR_001753740.2:n.1000G=
NM_000455.5:c.375G= MANE Select NP_000446.1:p.Met125=