Canonical Allele Identifier: CA046999
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 328228
dbSNP Id: rs774072752
gnomAD v2: 19-1206911-G-T
gnomAD v3: 19-1206912-G-T
gnomAD v4: 19-1206912-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1206912G>T , CM000681.2:g.1206912G>T GRCh38
NC_000019.9:g.1206911G>T , CM000681.1:g.1206911G>T GRCh37
NC_000019.8:g.1157911G>T NCBI36
NG_007460.2:g.22506G>T , LRG_319:g.22506G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.-2G>T ENSP00000490268.2:n.-2G>T
ENST00000585748.3:c.-82-11505G>T ENSP00000477641.2:n.-82-11505G>T
ENST00000585851.2:c.-2G>T ENSP00000467912.2:n.-2G>T
ENST00000326873.12:c.-2G>T MANE Select ENSP00000324856.6:n.-2G>T
ENST00000652231.1:c.-2G>T ENSP00000498804.1:n.-2G>T
ENST00000326873.11:c.-2G>T ENSP00000324856.6:n.-2G>T
ENST00000585748.2:c.-82-11505G>T ENSP00000477641.1:n.-82-11505G>T
ENST00000585851.1:c.-2G>T ENSP00000467912.1:n.-2G>T
ENST00000586243.5:c.-2G>T ENSP00000467240.2:n.-2G>T
ENST00000589152.5:n.89G>T
ENST00000593219.5:c.-2G>T ENSP00000466610.1:n.-2G>T
NM_000455.4:c.-2G>T , LRG_319t1:c.-2G>T NP_000446.1:n.-2G>T
XM_005259617.1:c.-2G>T XP_005259674.1:n.-2G>T
XM_005259618.3:c.-2G>T XP_005259675.1:n.-2G>T
XM_011528209.1:c.-355G>T XP_011526511.1:n.-355G>T
XR_936204.1:n.624G>T
XM_005259617.3:c.-2G>T XP_005259674.1:n.-2G>T
XM_011528209.2:c.-355G>T XP_011526511.1:n.-355G>T
XR_001753738.2:n.624G>T
XR_001753739.1:n.624G>T
XR_001753740.2:n.624G>T
NM_000455.5:c.-2G>T MANE Select NP_000446.1:n.-2G>T