Canonical Allele Identifier: CA402949472
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 527820
dbSNP Id: rs1555738370
gnomAD v3: 19-1220603-A-G
gnomAD v4: 19-1220603-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1220603A>G , CM000681.2:g.1220603A>G GRCh38
NC_000019.9:g.1220602A>G , CM000681.1:g.1220602A>G GRCh37
NC_000019.8:g.1171602A>G NCBI36
NG_007460.2:g.36197A>G , LRG_319:g.36197A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.620A>G ENSP00000490268.2:p.Asp207Gly
ENST00000585748.3:c.248A>G ENSP00000477641.2:p.Asp83Gly
ENST00000585851.2:c.446A>G ENSP00000467912.2:p.Asp149Gly
ENST00000326873.12:c.620A>G MANE Select ENSP00000324856.6:p.Asp207Gly
ENST00000652231.1:c.620A>G ENSP00000498804.1:p.Asp207Gly
ENST00000326873.11:c.620A>G ENSP00000324856.6:p.Asp207Gly
ENST00000585851.1:c.446A>G ENSP00000467912.1:p.Asp149Gly
ENST00000586243.5:c.620A>G ENSP00000467240.2:p.Asp207Gly
ENST00000586358.5:n.518A>G
ENST00000589152.5:n.710A>G
ENST00000591133.2:n.591A>G
NM_000455.4:c.620A>G , LRG_319t1:c.620A>G NP_000446.1:p.Asp207Gly
XM_005259617.1:c.620A>G XP_005259674.1:p.Asp207Gly
XM_005259618.3:c.620A>G XP_005259675.1:p.Asp207Gly
XM_011528209.1:c.398A>G XP_011526511.1:p.Asp133Gly
XR_936204.1:n.1245A>G
XM_005259617.3:c.620A>G XP_005259674.1:p.Asp207Gly
XM_011528209.2:c.398A>G XP_011526511.1:p.Asp133Gly
XR_001753738.2:n.1245A>G
XR_001753739.1:n.1245A>G
XR_001753740.2:n.1245A>G
NM_000455.5:c.620A>G MANE Select NP_000446.1:p.Asp207Gly