Canonical Allele Identifier: CA402954233
Gene: STK11 HGNC NCBI

Linked Data

dbSNP Id: rs757369900
gnomAD v4: 19-1226631-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1226631C>A , CM000681.2:g.1226631C>A GRCh38
NC_000019.9:g.1226630C>A , CM000681.1:g.1226630C>A GRCh37
NC_000019.8:g.1177630C>A NCBI36
NG_007460.2:g.42225C>A , LRG_319:g.42225C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000585465.3:c.*2887C>A ENSP00000490268.2:n.*2887C>A
ENST00000585748.3:c.914C>A ENSP00000477641.2:p.Ala305Asp
ENST00000585851.2:c.1112C>A ENSP00000467912.2:p.Ala371Asp
ENST00000326873.12:c.1286C>A MANE Select ENSP00000324856.6:p.Ala429Asp
ENST00000326873.11:c.1286C>A ENSP00000324856.6:p.Ala429Asp
ENST00000585465.2:n.3019C>A
ENST00000586243.5:c.1283C>A ENSP00000467240.2:p.Ala428Asp
ENST00000589152.5:n.1984C>A
NM_000455.4:c.1286C>A , LRG_319t1:c.1286C>A NP_000446.1:p.Ala429Asp
XM_005259617.1:c.1281C>A XP_005259674.1:p.Gly427=
XM_011528209.1:c.1059C>A XP_011526511.1:p.Gly353=
XM_005259617.3:c.1281C>A XP_005259674.1:p.Gly427=
XM_011528209.2:c.1059C>A XP_011526511.1:p.Gly353=
XR_001753738.2:n.2092C>A
XR_001753740.2:n.2062C>A
NM_000455.5:c.1286C>A MANE Select NP_000446.1:p.Ala429Asp