Canonical Allele Identifier: CA402947935
Gene: STK11 HGNC NCBI
ClinVar RCV:
ClinVar Variation:
MyVariant.info:
Revel Score:

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1218497A>C , CM000681.2:g.1218497A>C GRCh38
NC_000019.9:g.1218496A>C , CM000681.1:g.1218496A>C GRCh37
NC_000019.8:g.1169496A>C NCBI36
NG_007460.2:g.34091A>C , LRG_319:g.34091A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.371A>C ENSP00000490268.2:p.Lys124Thr
ENST00000585748.3:c.-2A>C ENSP00000477641.2:n.-2A>C
ENST00000585851.2:c.291-1876A>C ENSP00000467912.2:n.291-1876A>C
ENST00000326873.12:c.371A>C MANE Select ENSP00000324856.6:p.Lys124Thr
ENST00000652231.1:c.371A>C ENSP00000498804.1:p.Lys124Thr
ENST00000326873.11:c.371A>C ENSP00000324856.6:p.Lys124Thr
ENST00000585748.2:c.-2A>C ENSP00000477641.1:n.-2A>C
ENST00000585851.1:c.291-1876A>C ENSP00000467912.1:n.291-1876A>C
ENST00000586243.5:c.371A>C ENSP00000467240.2:p.Lys124Thr
ENST00000586358.5:n.194A>C
ENST00000589152.5:n.461A>C
ENST00000593219.5:c.*196A>C ENSP00000466610.1:n.*196A>C
NM_000455.4:c.371A>C , LRG_319t1:c.371A>C NP_000446.1:p.Lys124Thr
XM_005259617.1:c.371A>C XP_005259674.1:p.Lys124Thr
XM_005259618.3:c.371A>C XP_005259675.1:p.Lys124Thr
XM_011528209.1:c.149A>C XP_011526511.1:p.Lys50Thr
XR_936204.1:n.996A>C
XM_005259617.3:c.371A>C XP_005259674.1:p.Lys124Thr
XM_011528209.2:c.149A>C XP_011526511.1:p.Lys50Thr
XR_001753738.2:n.996A>C
XR_001753739.1:n.996A>C
XR_001753740.2:n.996A>C
NM_000455.5:c.371A>C MANE Select NP_000446.1:p.Lys124Thr