Canonical Allele Identifier: CA16616001
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 403766
ClinVar RCV Id: RCV000474390
dbSNP Id: rs1060499954

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1207025C>A , CM000681.2:g.1207025C>A GRCh38
NC_000019.9:g.1207024C>A , CM000681.1:g.1207024C>A GRCh37
NC_000019.8:g.1158024C>A NCBI36
NG_007460.2:g.22619C>A , LRG_319:g.22619C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.112C>A ENSP00000490268.2:p.Pro38Thr
ENST00000585748.3:c.-82-11392C>A ENSP00000477641.2:n.-82-11392C>A
ENST00000585851.2:c.112C>A ENSP00000467912.2:p.Pro38Thr
ENST00000326873.12:c.112C>A MANE Select ENSP00000324856.6:p.Pro38Thr
ENST00000652231.1:c.112C>A ENSP00000498804.1:p.Pro38Thr
ENST00000326873.11:c.112C>A ENSP00000324856.6:p.Pro38Thr
ENST00000585748.2:c.-82-11392C>A ENSP00000477641.1:n.-82-11392C>A
ENST00000585851.1:c.112C>A ENSP00000467912.1:p.Pro38Thr
ENST00000586243.5:c.112C>A ENSP00000467240.2:p.Pro38Thr
ENST00000589152.5:n.202C>A
ENST00000593219.5:c.112C>A ENSP00000466610.1:p.Pro38Thr
NM_000455.4:c.112C>A , LRG_319t1:c.112C>A NP_000446.1:p.Pro38Thr
XM_005259617.1:c.112C>A XP_005259674.1:p.Pro38Thr
XM_005259618.3:c.112C>A XP_005259675.1:p.Pro38Thr
XM_011528209.1:c.-242C>A XP_011526511.1:n.-242C>A
XR_936204.1:n.737C>A
XM_005259617.3:c.112C>A XP_005259674.1:p.Pro38Thr
XM_011528209.2:c.-242C>A XP_011526511.1:n.-242C>A
XR_001753738.2:n.737C>A
XR_001753739.1:n.737C>A
XR_001753740.2:n.737C>A
NM_000455.5:c.112C>A MANE Select NP_000446.1:p.Pro38Thr