Canonical Allele Identifier: CA631033964
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 458012
dbSNP Id: rs1407794756
gnomAD v2: 19-1226449-C-T
gnomAD v3: 19-1226450-C-T
gnomAD v4: 19-1226450-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1226450C>T , CM000681.2:g.1226450C>T GRCh38
NC_000019.9:g.1226449C>T , CM000681.1:g.1226449C>T GRCh37
NC_000019.8:g.1177449C>T NCBI36
NG_007460.2:g.42044C>T , LRG_319:g.42044C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.*2706C>T ENSP00000490268.2:n.*2706C>T
ENST00000585748.3:c.737-4C>T ENSP00000477641.2:n.737-4C>T
ENST00000585851.2:c.935-4C>T ENSP00000467912.2:n.935-4C>T
ENST00000326873.12:c.1109-4C>T MANE Select ENSP00000324856.6:n.1109-4C>T
ENST00000326873.11:c.1109-4C>T ENSP00000324856.6:n.1109-4C>T
ENST00000585465.2:n.2838C>T
ENST00000586243.5:c.1109-4C>T ENSP00000467240.2:n.1109-4C>T
ENST00000589152.5:n.1807-4C>T
NM_000455.4:c.1109-4C>T , LRG_319t1:c.1109-4C>T NP_000446.1:n.1109-4C>T
XM_005259617.1:c.1109-9C>T XP_005259674.1:n.1109-9C>T
XM_011528209.1:c.887-9C>T XP_011526511.1:n.887-9C>T
XM_005259617.3:c.1109-9C>T XP_005259674.1:n.1109-9C>T
XM_011528209.2:c.887-9C>T XP_011526511.1:n.887-9C>T
XR_001753738.2:n.1915-4C>T
XR_001753740.2:n.1885-4C>T
NM_000455.5:c.1109-4C>T MANE Select NP_000446.1:n.1109-4C>T