Canonical Allele Identifier: CA402942988
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1042673
dbSNP Id: rs1599914720
gnomAD v4: 19-1206924-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1206924T>C , CM000681.2:g.1206924T>C GRCh38
NC_000019.9:g.1206923T>C , CM000681.1:g.1206923T>C GRCh37
NC_000019.8:g.1157923T>C NCBI36
NG_007460.2:g.22518T>C , LRG_319:g.22518T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000585465.3:c.11T>C ENSP00000490268.2:p.Val4Ala
ENST00000585748.3:c.-82-11493T>C ENSP00000477641.2:n.-82-11493T>C
ENST00000585851.2:c.11T>C ENSP00000467912.2:p.Val4Ala
ENST00000326873.12:c.11T>C MANE Select ENSP00000324856.6:p.Val4Ala
ENST00000652231.1:c.11T>C ENSP00000498804.1:p.Val4Ala
ENST00000326873.11:c.11T>C ENSP00000324856.6:p.Val4Ala
ENST00000585748.2:c.-82-11493T>C ENSP00000477641.1:n.-82-11493T>C
ENST00000585851.1:c.11T>C ENSP00000467912.1:p.Val4Ala
ENST00000586243.5:c.11T>C ENSP00000467240.2:p.Val4Ala
ENST00000589152.5:n.101T>C
ENST00000593219.5:c.11T>C ENSP00000466610.1:p.Val4Ala
NM_000455.4:c.11T>C , LRG_319t1:c.11T>C NP_000446.1:p.Val4Ala
XM_005259617.1:c.11T>C XP_005259674.1:p.Val4Ala
XM_005259618.3:c.11T>C XP_005259675.1:p.Val4Ala
XM_011528209.1:c.-343T>C XP_011526511.1:n.-343T>C
XR_936204.1:n.636T>C
XM_005259617.3:c.11T>C XP_005259674.1:p.Val4Ala
XM_011528209.2:c.-343T>C XP_011526511.1:n.-343T>C
XR_001753738.2:n.636T>C
XR_001753739.1:n.636T>C
XR_001753740.2:n.636T>C
NM_000455.5:c.11T>C MANE Select NP_000446.1:p.Val4Ala