Canonical Allele Identifier: CA2317588579
Gene: STK11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1218507T= , CM000681.2:g.1218507T= GRCh38
NC_000019.9:g.1218506T= , CM000681.1:g.1218506T= GRCh37
NC_000019.8:g.1169506T= NCBI36
NG_007460.2:g.34101T= , LRG_319:g.34101T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.374+7T= ENSP00000490268.2:n.374+7T=
ENST00000585748.3:c.2+7T= ENSP00000477641.2:n.2+7T=
ENST00000585851.2:c.291-1866T= ENSP00000467912.2:n.291-1866T=
ENST00000326873.12:c.374+7T= MANE Select ENSP00000324856.6:n.374+7T=
ENST00000652231.1:c.374+7T= ENSP00000498804.1:n.374+7T=
ENST00000326873.11:c.374+7T= ENSP00000324856.6:n.374+7T=
ENST00000585748.2:c.2+7T= ENSP00000477641.1:n.2+7T=
ENST00000585851.1:c.291-1866T= ENSP00000467912.1:n.291-1866T=
ENST00000586243.5:c.374+7T= ENSP00000467240.2:n.374+7T=
ENST00000586358.5:n.197+7T=
ENST00000589152.5:n.464+7T=
ENST00000593219.5:c.*199+7T= ENSP00000466610.1:n.*199+7T=
NM_000455.4:c.374+7T= , LRG_319t1:c.374+7T= NP_000446.1:n.374+7T=
XM_005259617.1:c.374+7T= XP_005259674.1:n.374+7T=
XM_005259618.3:c.374+7T= XP_005259675.1:n.374+7T=
XM_011528209.1:c.152+7T= XP_011526511.1:n.152+7T=
XR_936204.1:n.999+7T=
XM_005259617.3:c.374+7T= XP_005259674.1:n.374+7T=
XM_011528209.2:c.152+7T= XP_011526511.1:n.152+7T=
XR_001753738.2:n.999+7T=
XR_001753739.1:n.999+7T=
XR_001753740.2:n.999+7T=
NM_000455.5:c.374+7T= MANE Select NP_000446.1:n.374+7T=