Canonical Allele Identifier: CA2317588434

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218269_1218285delinsTCCCACAGCACTGTGAA , CM000681.2:g.1218269_1218285delinsTCCCACAGCACTGTGAA	GRCh38
NC_000019.9:g.1218268_1218284delinsTCCCACAGCACTGTGAA , CM000681.1:g.1218268_1218284delinsTCCCACAGCACTGTGAA	GRCh37
NC_000019.8:g.1169268_1169284delinsTCCCACAGCACTGTGAA	NCBI36
NG_007460.2:g.33863_33879delinsTCCCACAGCACTGTGAA , LRG_319:g.33863_33879delinsTCCCACAGCACTGTGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.291-148_291-132delinsTCCCACAGCACTGTGAA	ENSP00000490268.2:n.291-148_291-132delinsTCCCACAGCACTGTGAA
ENST00000585748.3:c.-82-148_-82-132delinsTCCCACAGCACTGTGAA	ENSP00000477641.2:n.-82-148_-82-132delinsTCCCACAGCACTGTGAA
ENST00000585851.2:c.291-2104_291-2088delinsTCCCACAGCACTGTGAA	ENSP00000467912.2:n.291-2104_291-2088delinsTCCCACAGCACTGTGAA
ENST00000326873.12:c.291-148_291-132delinsTCCCACAGCACTGTGAA MANE Select	ENSP00000324856.6:n.291-148_291-132delinsTCCCACAGCACTGTGAA
ENST00000652231.1:c.291-148_291-132delinsTCCCACAGCACTGTGAA	ENSP00000498804.1:n.291-148_291-132delinsTCCCACAGCACTGTGAA
ENST00000326873.11:c.291-148_291-132delinsTCCCACAGCACTGTGAA	ENSP00000324856.6:n.291-148_291-132delinsTCCCACAGCACTGTGAA
ENST00000585748.2:c.-82-148_-82-132delinsTCCCACAGCACTGTGAA	ENSP00000477641.1:n.-82-148_-82-132delinsTCCCACAGCACTGTGAA
ENST00000585851.1:c.291-2104_291-2088delinsTCCCACAGCACTGTGAA	ENSP00000467912.1:n.291-2104_291-2088delinsTCCCACAGCACTGTGAA
ENST00000586243.5:c.291-148_291-132delinsTCCCACAGCACTGTGAA	ENSP00000467240.2:n.291-148_291-132delinsTCCCACAGCACTGTGAA
ENST00000586358.5:n.114-148_114-132delinsTCCCACAGCACTGTGAA
ENST00000589152.5:n.381-148_381-132delinsTCCCACAGCACTGTGAA
ENST00000593219.5:c.*116-148_*116-132delinsTCCCACAGCACTGTGAA	ENSP00000466610.1:n.*116-148_*116-132delinsTCCCACAGCACTGTGAA
NM_000455.4:c.291-148_291-132delinsTCCCACAGCACTGTGAA , LRG_319t1:c.291-148_291-132delinsTCCCACAGCACTGTGAA	NP_000446.1:n.291-148_291-132delinsTCCCACAGCACTGTGAA
XM_005259617.1:c.291-148_291-132delinsTCCCACAGCACTGTGAA	XP_005259674.1:n.291-148_291-132delinsTCCCACAGCACTGTGAA
XM_005259618.3:c.291-148_291-132delinsTCCCACAGCACTGTGAA	XP_005259675.1:n.291-148_291-132delinsTCCCACAGCACTGTGAA
XM_011528209.1:c.69-148_69-132delinsTCCCACAGCACTGTGAA	XP_011526511.1:n.69-148_69-132delinsTCCCACAGCACTGTGAA
XR_936204.1:n.916-148_916-132delinsTCCCACAGCACTGTGAA
XM_005259617.3:c.291-148_291-132delinsTCCCACAGCACTGTGAA	XP_005259674.1:n.291-148_291-132delinsTCCCACAGCACTGTGAA
XM_011528209.2:c.69-148_69-132delinsTCCCACAGCACTGTGAA	XP_011526511.1:n.69-148_69-132delinsTCCCACAGCACTGTGAA
XR_001753738.2:n.916-148_916-132delinsTCCCACAGCACTGTGAA
XR_001753739.1:n.916-148_916-132delinsTCCCACAGCACTGTGAA
XR_001753740.2:n.916-148_916-132delinsTCCCACAGCACTGTGAA
NM_000455.5:c.291-148_291-132delinsTCCCACAGCACTGTGAA MANE Select	NP_000446.1:n.291-148_291-132delinsTCCCACAGCACTGTGAA