Canonical Allele Identifier: CA402951543
Gene: STK11 HGNC NCBI

Linked Data

dbSNP Id: rs781528711

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1223023T>A , CM000681.2:g.1223023T>A GRCh38
NC_000019.9:g.1223022T>A , CM000681.1:g.1223022T>A GRCh37
NC_000019.8:g.1174022T>A NCBI36
NG_007460.2:g.38617T>A , LRG_319:g.38617T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.959T>A ENSP00000490268.2:p.Val320Glu
ENST00000585748.3:c.587T>A ENSP00000477641.2:p.Val196Glu
ENST00000585851.2:c.785T>A ENSP00000467912.2:p.Val262Glu
ENST00000326873.12:c.959T>A MANE Select ENSP00000324856.6:p.Val320Glu
ENST00000652231.1:c.959T>A ENSP00000498804.1:p.Val320Glu
ENST00000326873.11:c.959T>A ENSP00000324856.6:p.Val320Glu
ENST00000586243.5:c.959T>A ENSP00000467240.2:p.Val320Glu
ENST00000589152.5:n.1657T>A
ENST00000591133.2:n.930T>A
NM_000455.4:c.959T>A , LRG_319t1:c.959T>A NP_000446.1:p.Val320Glu
XM_005259617.1:c.959T>A XP_005259674.1:p.Val320Glu
XM_005259618.3:c.959T>A XP_005259675.1:p.Val320Glu
XM_011528209.1:c.737T>A XP_011526511.1:p.Val246Glu
XR_936204.1:n.1735T>A
XM_005259617.3:c.959T>A XP_005259674.1:p.Val320Glu
XM_011528209.2:c.737T>A XP_011526511.1:p.Val246Glu
XR_001753738.2:n.1765T>A
XR_001753739.1:n.1765T>A
XR_001753740.2:n.1735T>A
NM_000455.5:c.959T>A MANE Select NP_000446.1:p.Val320Glu