Canonical Allele Identifier: CA023391
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 184692
dbSNP Id: rs771632414
gnomAD v2: 19-1223039-C-A
gnomAD v3: 19-1223040-C-A
gnomAD v4: 19-1223040-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1223040C>A , CM000681.2:g.1223040C>A GRCh38
NC_000019.9:g.1223039C>A , CM000681.1:g.1223039C>A GRCh37
NC_000019.8:g.1174039C>A NCBI36
NG_007460.2:g.38634C>A , LRG_319:g.38634C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.976C>A ENSP00000490268.2:p.Pro326Thr
ENST00000585748.3:c.604C>A ENSP00000477641.2:p.Pro202Thr
ENST00000585851.2:c.802C>A ENSP00000467912.2:p.Pro268Thr
ENST00000326873.12:c.976C>A MANE Select ENSP00000324856.6:p.Pro326Thr
ENST00000652231.1:c.976C>A ENSP00000498804.1:p.Pro326Thr
ENST00000326873.11:c.976C>A ENSP00000324856.6:p.Pro326Thr
ENST00000586243.5:c.976C>A ENSP00000467240.2:p.Pro326Thr
ENST00000589152.5:n.1674C>A
ENST00000591133.2:n.947C>A
NM_000455.4:c.976C>A , LRG_319t1:c.976C>A NP_000446.1:p.Pro326Thr
XM_005259617.1:c.976C>A XP_005259674.1:p.Pro326Thr
XM_005259618.3:c.976C>A XP_005259675.1:p.Pro326Thr
XM_011528209.1:c.754C>A XP_011526511.1:p.Pro252Thr
XR_936204.1:n.1752C>A
XM_005259617.3:c.976C>A XP_005259674.1:p.Pro326Thr
XM_011528209.2:c.754C>A XP_011526511.1:p.Pro252Thr
XR_001753738.2:n.1782C>A
XR_001753739.1:n.1782C>A
XR_001753740.2:n.1752C>A
NM_000455.5:c.976C>A MANE Select NP_000446.1:p.Pro326Thr