Canonical Allele Identifier: CA023320
Gene: STK11 HGNC NCBI
ClinVar Variation:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1221963G>A , CM000681.2:g.1221963G>A GRCh38
NC_000019.9:g.1221962G>A , CM000681.1:g.1221962G>A GRCh37
NC_000019.8:g.1172962G>A NCBI36
NG_007460.2:g.37557G>A , LRG_319:g.37557G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.877G>A ENSP00000490268.2:p.Glu293Lys
ENST00000585748.3:c.505G>A ENSP00000477641.2:p.Glu169Lys
ENST00000585851.2:c.703G>A ENSP00000467912.2:p.Glu235Lys
ENST00000326873.12:c.877G>A MANE Select ENSP00000324856.6:p.Glu293Lys
ENST00000652231.1:c.877G>A ENSP00000498804.1:p.Glu293Lys
ENST00000326873.11:c.877G>A ENSP00000324856.6:p.Glu293Lys
ENST00000586243.5:c.877G>A ENSP00000467240.2:p.Glu293Lys
ENST00000589152.5:n.1575G>A
ENST00000591133.2:n.848G>A
NM_000455.4:c.877G>A , LRG_319t1:c.877G>A NP_000446.1:p.Glu293Lys
XM_005259617.1:c.877G>A XP_005259674.1:p.Glu293Lys
XM_005259618.3:c.877G>A XP_005259675.1:p.Glu293Lys
XM_011528209.1:c.655G>A XP_011526511.1:p.Glu219Lys
XR_936204.1:n.1653G>A
XM_005259617.3:c.877G>A XP_005259674.1:p.Glu293Lys
XM_011528209.2:c.655G>A XP_011526511.1:p.Glu219Lys
XR_001753738.2:n.1683G>A
XR_001753739.1:n.1683G>A
XR_001753740.2:n.1653G>A
NM_000455.5:c.877G>A MANE Select NP_000446.1:p.Glu293Lys