Canonical Allele Identifier: CA023012
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 142377
dbSNP Id: rs373167735
gnomAD v2: 19-1219416-C-T
gnomAD v3: 19-1219417-C-T
gnomAD v4: 19-1219417-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1219417C>T , CM000681.2:g.1219417C>T GRCh38
NC_000019.9:g.1219416C>T , CM000681.1:g.1219416C>T GRCh37
NC_000019.8:g.1170416C>T NCBI36
NG_007460.2:g.35011C>T , LRG_319:g.35011C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000585465.3:c.464+4C>T ENSP00000490268.2:n.464+4C>T
ENST00000585748.3:c.92+4C>T ENSP00000477641.2:n.92+4C>T
ENST00000585851.2:c.291-956C>T ENSP00000467912.2:n.291-956C>T
ENST00000326873.12:c.464+4C>T MANE Select ENSP00000324856.6:n.464+4C>T
ENST00000652231.1:c.464+4C>T ENSP00000498804.1:n.464+4C>T
ENST00000326873.11:c.464+4C>T ENSP00000324856.6:n.464+4C>T
ENST00000585851.1:c.291-956C>T ENSP00000467912.1:n.291-956C>T
ENST00000586243.5:c.464+4C>T ENSP00000467240.2:n.464+4C>T
ENST00000586358.5:n.287+4C>T
ENST00000589152.5:n.554+4C>T
NM_000455.4:c.464+4C>T , LRG_319t1:c.464+4C>T NP_000446.1:n.464+4C>T
XM_005259617.1:c.464+4C>T XP_005259674.1:n.464+4C>T
XM_005259618.3:c.464+4C>T XP_005259675.1:n.464+4C>T
XM_011528209.1:c.242+4C>T XP_011526511.1:n.242+4C>T
XR_936204.1:n.1089+4C>T
XM_005259617.3:c.464+4C>T XP_005259674.1:n.464+4C>T
XM_011528209.2:c.242+4C>T XP_011526511.1:n.242+4C>T
XR_001753738.2:n.1089+4C>T
XR_001753739.1:n.1089+4C>T
XR_001753740.2:n.1089+4C>T
NM_000455.5:c.464+4C>T MANE Select NP_000446.1:n.464+4C>T