Canonical Allele Identifier: CA022704
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 185127
dbSNP Id: rs759284466

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1206913C>T , CM000681.2:g.1206913C>T GRCh38
NC_000019.9:g.1206912C>T , CM000681.1:g.1206912C>T GRCh37
NC_000019.8:g.1157912C>T NCBI36
NG_007460.2:g.22507C>T , LRG_319:g.22507C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000326873.12:c.-1C>T MANE Select ENSP00000324856.6:p.=
ENST00000652231.1:c.-1C>T ENSP00000498804.1:p.=
ENST00000326873.11:c.-1C>T ENSP00000324856.6:p.=
ENST00000585748.2:c.-82-11504C>T ENSP00000477641.1:p.=
ENST00000585851.1:c.-1C>T ENSP00000467912.1:p.=
ENST00000586243.5:c.-1C>T ENSP00000467240.2:p.=
ENST00000589152.5:n.90C>T
ENST00000593219.5:c.-1C>T ENSP00000466610.1:p.=
NM_000455.4:c.-1C>T , LRG_319t1:c.-1C>T NP_000446.1:p.=
XM_005259617.1:c.-1C>T XP_005259674.1:p.=
XM_005259618.3:c.-1C>T XP_005259675.1:p.=
XM_011528209.1:c.-354C>T XP_011526511.1:p.=
XR_936204.1:n.625C>T
XM_005259617.3:c.-1C>T XP_005259674.1:p.=
XM_011528209.2:c.-354C>T XP_011526511.1:p.=
XR_001753738.2:n.625C>T
XR_001753739.1:n.625C>T
XR_001753740.2:n.625C>T
NM_000455.5:c.-1C>T MANE Select NP_000446.1:p.=