Canonical Allele Identifier: CA022954
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 135922
dbSNP Id: rs587780718
gnomAD v2: 19-1219395-A-G
gnomAD v3: 19-1219396-A-G
gnomAD v4: 19-1219396-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1219396A>G , CM000681.2:g.1219396A>G GRCh38
NC_000019.9:g.1219395A>G , CM000681.1:g.1219395A>G GRCh37
NC_000019.8:g.1170395A>G NCBI36
NG_007460.2:g.34990A>G , LRG_319:g.34990A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.447A>G ENSP00000490268.2:p.Pro149=
ENST00000585748.3:c.75A>G ENSP00000477641.2:p.Pro25=
ENST00000585851.2:c.291-977A>G ENSP00000467912.2:n.291-977A>G
ENST00000326873.12:c.447A>G MANE Select ENSP00000324856.6:p.Pro149=
ENST00000652231.1:c.447A>G ENSP00000498804.1:p.Pro149=
ENST00000326873.11:c.447A>G ENSP00000324856.6:p.Pro149=
ENST00000585851.1:c.291-977A>G ENSP00000467912.1:n.291-977A>G
ENST00000586243.5:c.447A>G ENSP00000467240.2:p.Pro149=
ENST00000586358.5:n.270A>G
ENST00000589152.5:n.537A>G
NM_000455.4:c.447A>G , LRG_319t1:c.447A>G NP_000446.1:p.Pro149=
XM_005259617.1:c.447A>G XP_005259674.1:p.Pro149=
XM_005259618.3:c.447A>G XP_005259675.1:p.Pro149=
XM_011528209.1:c.225A>G XP_011526511.1:p.Pro75=
XR_936204.1:n.1072A>G
XM_005259617.3:c.447A>G XP_005259674.1:p.Pro149=
XM_011528209.2:c.225A>G XP_011526511.1:p.Pro75=
XR_001753738.2:n.1072A>G
XR_001753739.1:n.1072A>G
XR_001753740.2:n.1072A>G
NM_000455.5:c.447A>G MANE Select NP_000446.1:p.Pro149=