Canonical Allele Identifier: CA2317588419

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218249_1218268delinsGTGGCCCCTGCAGGGCCCTT , CM000681.2:g.1218249_1218268delinsGTGGCCCCTGCAGGGCCCTT	GRCh38
NC_000019.9:g.1218248_1218267delinsGTGGCCCCTGCAGGGCCCTT , CM000681.1:g.1218248_1218267delinsGTGGCCCCTGCAGGGCCCTT	GRCh37
NC_000019.8:g.1169248_1169267delinsGTGGCCCCTGCAGGGCCCTT	NCBI36
NG_007460.2:g.33843_33862delinsGTGGCCCCTGCAGGGCCCTT , LRG_319:g.33843_33862delinsGTGGCCCCTGCAGGGCCCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.291-168_291-149delinsGTGGCCCCTGCAGGGCCCTT	ENSP00000490268.2:n.291-168_291-149delinsGTGGCCCCTGCAGGGCCCTT...
ENST00000585748.3:c.-82-168_-82-149delinsGTGGCCCCTGCAGGGCCCTT	ENSP00000477641.2:n.-82-168_-82-149delinsGTGGCCCCTGCAGGGCCCTT...
ENST00000585851.2:c.291-2124_291-2105delinsGTGGCCCCTGCAGGGCCCTT	ENSP00000467912.2:n.291-2124_291-2105delinsGTGGCCCCTGCAGGGCCC...
ENST00000326873.12:c.291-168_291-149delinsGTGGCCCCTGCAGGGCCCTT MANE Select	ENSP00000324856.6:n.291-168_291-149delinsGTGGCCCCTGCAGGGCCCTT...
ENST00000652231.1:c.291-168_291-149delinsGTGGCCCCTGCAGGGCCCTT	ENSP00000498804.1:n.291-168_291-149delinsGTGGCCCCTGCAGGGCCCTT...
ENST00000326873.11:c.291-168_291-149delinsGTGGCCCCTGCAGGGCCCTT	ENSP00000324856.6:n.291-168_291-149delinsGTGGCCCCTGCAGGGCCCTT...
ENST00000585748.2:c.-82-168_-82-149delinsGTGGCCCCTGCAGGGCCCTT	ENSP00000477641.1:n.-82-168_-82-149delinsGTGGCCCCTGCAGGGCCCTT...
ENST00000585851.1:c.291-2124_291-2105delinsGTGGCCCCTGCAGGGCCCTT	ENSP00000467912.1:n.291-2124_291-2105delinsGTGGCCCCTGCAGGGCCC...
ENST00000586243.5:c.291-168_291-149delinsGTGGCCCCTGCAGGGCCCTT	ENSP00000467240.2:n.291-168_291-149delinsGTGGCCCCTGCAGGGCCCTT...
ENST00000586358.5:n.114-168_114-149delinsGTGGCCCCTGCAGGGCCCTT
ENST00000589152.5:n.381-168_381-149delinsGTGGCCCCTGCAGGGCCCTT
ENST00000593219.5:c.*116-168_*116-149delinsGTGGCCCCTGCAGGGCCCTT	ENSP00000466610.1:n.*116-168_*116-149delinsGTGGCCCCTGCAGGGCCC...
NM_000455.4:c.291-168_291-149delinsGTGGCCCCTGCAGGGCCCTT , LRG_319t1:c.291-168_291-149delinsGTGGCCCCTGCAGGGCCCTT	NP_000446.1:n.291-168_291-149delinsGTGGCCCCTGCAGGGCCCTT
XM_005259617.1:c.291-168_291-149delinsGTGGCCCCTGCAGGGCCCTT	XP_005259674.1:n.291-168_291-149delinsGTGGCCCCTGCAGGGCCCTT
XM_005259618.3:c.291-168_291-149delinsGTGGCCCCTGCAGGGCCCTT	XP_005259675.1:n.291-168_291-149delinsGTGGCCCCTGCAGGGCCCTT
XM_011528209.1:c.69-168_69-149delinsGTGGCCCCTGCAGGGCCCTT	XP_011526511.1:n.69-168_69-149delinsGTGGCCCCTGCAGGGCCCTT
XR_936204.1:n.916-168_916-149delinsGTGGCCCCTGCAGGGCCCTT
XM_005259617.3:c.291-168_291-149delinsGTGGCCCCTGCAGGGCCCTT	XP_005259674.1:n.291-168_291-149delinsGTGGCCCCTGCAGGGCCCTT
XM_011528209.2:c.69-168_69-149delinsGTGGCCCCTGCAGGGCCCTT	XP_011526511.1:n.69-168_69-149delinsGTGGCCCCTGCAGGGCCCTT
XR_001753738.2:n.916-168_916-149delinsGTGGCCCCTGCAGGGCCCTT
XR_001753739.1:n.916-168_916-149delinsGTGGCCCCTGCAGGGCCCTT
XR_001753740.2:n.916-168_916-149delinsGTGGCCCCTGCAGGGCCCTT
NM_000455.5:c.291-168_291-149delinsGTGGCCCCTGCAGGGCCCTT MANE Select	NP_000446.1:n.291-168_291-149delinsGTGGCCCCTGCAGGGCCCTT