Canonical Allele Identifier: CA783273800
Gene: STK11 HGNC NCBI

Linked Data

dbSNP Id: rs1455952691

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1207332_1207336dup , CM000681.2:g.1207332_1207336dup GRCh38
NC_000019.9:g.1207331_1207335dup , CM000681.1:g.1207331_1207335dup GRCh37
NC_000019.8:g.1158331_1158335dup NCBI36
NG_007460.2:g.22926_22930dup , LRG_319:g.22926_22930dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.290+129_290+133dup ENSP00000490268.2:n.290+129_290+133dup
ENST00000585748.3:c.-82-11085_-82-11081dup ENSP00000477641.2:n.-82-11085_-82-11081dup
ENST00000585851.2:c.290+129_290+133dup ENSP00000467912.2:n.290+129_290+133dup
ENST00000326873.12:c.290+129_290+133dup MANE Select ENSP00000324856.6:n.290+129_290+133dup
ENST00000652231.1:c.290+129_290+133dup ENSP00000498804.1:n.290+129_290+133dup
ENST00000326873.11:c.290+129_290+133dup ENSP00000324856.6:n.290+129_290+133dup
ENST00000585748.2:c.-82-11085_-82-11081dup ENSP00000477641.1:n.-82-11085_-82-11081dup
ENST00000585851.1:c.290+129_290+133dup ENSP00000467912.1:n.290+129_290+133dup
ENST00000586243.5:c.290+129_290+133dup ENSP00000467240.2:n.290+129_290+133dup
ENST00000586358.5:n.113+129_113+133dup
ENST00000589152.5:n.380+129_380+133dup
ENST00000593219.5:c.290+129_290+133dup ENSP00000466610.1:n.290+129_290+133dup
NM_000455.4:c.290+129_290+133dup , LRG_319t1:c.290+129_290+133dup NP_000446.1:n.290+129_290+133dup
XM_005259617.1:c.290+129_290+133dup XP_005259674.1:n.290+129_290+133dup
XM_005259618.3:c.290+129_290+133dup XP_005259675.1:n.290+129_290+133dup
XM_011528209.1:c.-64+129_-64+133dup XP_011526511.1:n.-64+129_-64+133dup
XR_936204.1:n.915+129_915+133dup
XM_005259617.3:c.290+129_290+133dup XP_005259674.1:n.290+129_290+133dup
XM_011528209.2:c.-64+129_-64+133dup XP_011526511.1:n.-64+129_-64+133dup
XR_001753738.2:n.915+129_915+133dup
XR_001753739.1:n.915+129_915+133dup
XR_001753740.2:n.915+129_915+133dup
NM_000455.5:c.290+129_290+133dup MANE Select NP_000446.1:n.290+129_290+133dup