Canonical Allele Identifier: CA992489437
Gene: STK11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1218143_1218144insAAAA , CM000681.2:g.1218143_1218144insAAAA GRCh38
NC_000019.9:g.1218142_1218143insAAAA , CM000681.1:g.1218142_1218143insAAAA GRCh37
NC_000019.8:g.1169142_1169143insAAAA NCBI36
NG_007460.2:g.33737_33738insAAAA , LRG_319:g.33737_33738insAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.291-274_291-273insAAAA ENSP00000490268.2:n.291-274_291-273insAAAA
ENST00000585748.3:c.-82-274_-82-273insAAAA ENSP00000477641.2:n.-82-274_-82-273insAAAA
ENST00000585851.2:c.291-2230_291-2229insAAAA ENSP00000467912.2:n.291-2230_291-2229insAAAA
ENST00000326873.12:c.291-274_291-273insAAAA MANE Select ENSP00000324856.6:n.291-274_291-273insAAAA
ENST00000652231.1:c.291-274_291-273insAAAA ENSP00000498804.1:n.291-274_291-273insAAAA
ENST00000326873.11:c.291-274_291-273insAAAA ENSP00000324856.6:n.291-274_291-273insAAAA
ENST00000585748.2:c.-82-274_-82-273insAAAA ENSP00000477641.1:n.-82-274_-82-273insAAAA
ENST00000585851.1:c.291-2230_291-2229insAAAA ENSP00000467912.1:n.291-2230_291-2229insAAAA
ENST00000586243.5:c.291-274_291-273insAAAA ENSP00000467240.2:n.291-274_291-273insAAAA
ENST00000586358.5:n.114-274_114-273insAAAA
ENST00000589152.5:n.381-274_381-273insAAAA
ENST00000593219.5:c.*116-274_*116-273insAAAA ENSP00000466610.1:n.*116-274_*116-273insAAAA
NM_000455.4:c.291-274_291-273insAAAA , LRG_319t1:c.291-274_291-273insAAAA NP_000446.1:n.291-274_291-273insAAAA
XM_005259617.1:c.291-274_291-273insAAAA XP_005259674.1:n.291-274_291-273insAAAA
XM_005259618.3:c.291-274_291-273insAAAA XP_005259675.1:n.291-274_291-273insAAAA
XM_011528209.1:c.69-274_69-273insAAAA XP_011526511.1:n.69-274_69-273insAAAA
XR_936204.1:n.916-274_916-273insAAAA
XM_005259617.3:c.291-274_291-273insAAAA XP_005259674.1:n.291-274_291-273insAAAA
XM_011528209.2:c.69-274_69-273insAAAA XP_011526511.1:n.69-274_69-273insAAAA
XR_001753738.2:n.916-274_916-273insAAAA
XR_001753739.1:n.916-274_916-273insAAAA
XR_001753740.2:n.916-274_916-273insAAAA
NM_000455.5:c.291-274_291-273insAAAA MANE Select NP_000446.1:n.291-274_291-273insAAAA