Canonical Allele Identifier: CA645369764
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 428758
ClinVar RCV Id: RCV000492215
dbSNP Id: rs1131690922

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1220405_1220408dup , CM000681.2:g.1220405_1220408dup GRCh38
NC_000019.9:g.1220404_1220407dup , CM000681.1:g.1220404_1220407dup GRCh37
NC_000019.8:g.1171404_1171407dup NCBI36
NG_007460.2:g.35999_36002dup , LRG_319:g.35999_36002dup

Transcript Alleles

HGVS Amino-acid change
ENST00000585465.3:c.497_500dup ENSP00000490268.2:p.His168ProfsTer3
ENST00000585748.3:c.125_128dup ENSP00000477641.2:p.His44ProfsTer3
ENST00000585851.2:c.323_326dup ENSP00000467912.2:p.His110ProfsTer3
ENST00000326873.12:c.497_500dup MANE Select ENSP00000324856.6:p.His168ProfsTer3
ENST00000652231.1:c.497_500dup ENSP00000498804.1:p.His168ProfsTer3
ENST00000326873.11:c.497_500dup ENSP00000324856.6:p.His168ProfsTer3
ENST00000585851.1:c.323_326dup ENSP00000467912.1:p.His110ProfsTer3
ENST00000586243.5:c.497_500dup ENSP00000467240.2:p.His168ProfsTer3
ENST00000586358.5:n.320_323dup
ENST00000589152.5:n.587_590dup
ENST00000591133.2:n.393_396dup
NM_000455.4:c.497_500dup , LRG_319t1:c.497_500dup NP_000446.1:p.His168ProfsTer3
XM_005259617.1:c.497_500dup XP_005259674.1:p.His168ProfsTer3
XM_005259618.3:c.497_500dup XP_005259675.1:p.His168ProfsTer3
XM_011528209.1:c.275_278dup XP_011526511.1:p.His94ProfsTer3
XR_936204.1:n.1122_1125dup
XM_005259617.3:c.497_500dup XP_005259674.1:p.His168ProfsTer3
XM_011528209.2:c.275_278dup XP_011526511.1:p.His94ProfsTer3
XR_001753738.2:n.1122_1125dup
XR_001753739.1:n.1122_1125dup
XR_001753740.2:n.1122_1125dup
NM_000455.5:c.497_500dup MANE Select NP_000446.1:p.His168ProfsTer3