Canonical Allele Identifier: CA402950667
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1762904
ClinVar RCV Id: RCV002430415
dbSNP Id: rs1555738693
gnomAD v4: 19-1221309-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1221309C>G , CM000681.2:g.1221309C>G GRCh38
NC_000019.9:g.1221308C>G , CM000681.1:g.1221308C>G GRCh37
NC_000019.8:g.1172308C>G NCBI36
NG_007460.2:g.36903C>G , LRG_319:g.36903C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.831C>G ENSP00000490268.2:p.Asp277Glu
ENST00000585748.3:c.459C>G ENSP00000477641.2:p.Asp153Glu
ENST00000585851.2:c.657C>G ENSP00000467912.2:p.Asp219Glu
ENST00000326873.12:c.831C>G MANE Select ENSP00000324856.6:p.Asp277Glu
ENST00000652231.1:c.831C>G ENSP00000498804.1:p.Asp277Glu
ENST00000326873.11:c.831C>G ENSP00000324856.6:p.Asp277Glu
ENST00000586243.5:c.831C>G ENSP00000467240.2:p.Asp277Glu
ENST00000586358.5:n.729C>G
ENST00000589152.5:n.921C>G
ENST00000591133.2:n.802C>G
NM_000455.4:c.831C>G , LRG_319t1:c.831C>G NP_000446.1:p.Asp277Glu
XM_005259617.1:c.831C>G XP_005259674.1:p.Asp277Glu
XM_005259618.3:c.831C>G XP_005259675.1:p.Asp277Glu
XM_011528209.1:c.609C>G XP_011526511.1:p.Asp203Glu
XR_936204.1:n.1456C>G
XM_005259617.3:c.831C>G XP_005259674.1:p.Asp277Glu
XM_011528209.2:c.609C>G XP_011526511.1:p.Asp203Glu
XR_001753738.2:n.1456C>G
XR_001753739.1:n.1456C>G
XR_001753740.2:n.1456C>G
NM_000455.5:c.831C>G MANE Select NP_000446.1:p.Asp277Glu