Canonical Allele Identifier: CA402953898
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 485003
ClinVar RCV Id: RCV000575038
dbSNP Id: rs1555740221
gnomAD v4: 19-1226578-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1226578C>A , CM000681.2:g.1226578C>A GRCh38
NC_000019.9:g.1226577C>A , CM000681.1:g.1226577C>A GRCh37
NC_000019.8:g.1177577C>A NCBI36
NG_007460.2:g.42172C>A , LRG_319:g.42172C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.*2834C>A ENSP00000490268.2:n.*2834C>A
ENST00000585748.3:c.861C>A ENSP00000477641.2:p.Pro287=
ENST00000585851.2:c.1059C>A ENSP00000467912.2:p.Pro353=
ENST00000326873.12:c.1233C>A MANE Select ENSP00000324856.6:p.Pro411=
ENST00000326873.11:c.1233C>A ENSP00000324856.6:p.Pro411=
ENST00000585465.2:n.2966C>A
ENST00000586243.5:c.1232C>A ENSP00000467240.2:p.Pro411Gln
ENST00000589152.5:n.1931C>A
NM_000455.4:c.1233C>A , LRG_319t1:c.1233C>A NP_000446.1:p.Pro411=
XM_005259617.1:c.1228C>A XP_005259674.1:p.Gln410Lys
XM_011528209.1:c.1006C>A XP_011526511.1:p.Gln336Lys
XM_005259617.3:c.1228C>A XP_005259674.1:p.Gln410Lys
XM_011528209.2:c.1006C>A XP_011526511.1:p.Gln336Lys
XR_001753738.2:n.2039C>A
XR_001753740.2:n.2009C>A
NM_000455.5:c.1233C>A MANE Select NP_000446.1:p.Pro411=