Canonical Allele Identifier: CA2582591143
Gene: STK11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1206796_1206797insT , CM000681.2:g.1206796_1206797insT GRCh38
NC_000019.9:g.1206795_1206796insT , CM000681.1:g.1206795_1206796insT GRCh37
NC_000019.8:g.1157795_1157796insT NCBI36
NG_007460.2:g.22390_22391insT , LRG_319:g.22390_22391insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.-118_-117insT ENSP00000490268.2:n.-118_-117insT
ENST00000585748.3:c.-82-11621_-82-11620insT ENSP00000477641.2:n.-82-11621_-82-11620insT
ENST00000326873.12:c.-118_-117insT MANE Select ENSP00000324856.6:n.-118_-117insT
ENST00000652231.1:c.-118_-117insT ENSP00000498804.1:n.-118_-117insT
ENST00000326873.11:c.-118_-117insT ENSP00000324856.6:n.-118_-117insT
ENST00000585748.2:c.-82-11621_-82-11620insT ENSP00000477641.1:n.-82-11621_-82-11620insT
ENST00000586243.5:c.-118_-117insT ENSP00000467240.2:n.-118_-117insT
NM_000455.4:c.-118_-117insT , LRG_319t1:c.-118_-117insT NP_000446.1:n.-118_-117insT
XM_005259617.1:c.-118_-117insT XP_005259674.1:n.-118_-117insT
XM_005259618.3:c.-118_-117insT XP_005259675.1:n.-118_-117insT
XM_011528209.1:c.-471_-470insT XP_011526511.1:n.-471_-470insT
XR_936204.1:n.508_509insT
XM_005259617.3:c.-118_-117insT XP_005259674.1:n.-118_-117insT
XM_011528209.2:c.-471_-470insT XP_011526511.1:n.-471_-470insT
XR_001753738.2:n.508_509insT
XR_001753739.1:n.508_509insT
XR_001753740.2:n.508_509insT
NM_000455.5:c.-118_-117insT MANE Select NP_000446.1:n.-118_-117insT