Canonical Allele Identifier: CA2317588340

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218126_1218153delinsGAGCAAGACTCTGTCTCAGAAAAAAAAA , CM000681.2:g.1218126_1218153delinsGAGCAAGACTCTGTCTCAGAAAAAAAAA	GRCh38
NC_000019.9:g.1218125_1218152delinsGAGCAAGACTCTGTCTCAGAAAAAAAAA , CM000681.1:g.1218125_1218152delinsGAGCAAGACTCTGTCTCAGAAAAAAAAA	GRCh37
NC_000019.8:g.1169125_1169152delinsGAGCAAGACTCTGTCTCAGAAAAAAAAA	NCBI36
NG_007460.2:g.33720_33747delinsGAGCAAGACTCTGTCTCAGAAAAAAAAA , LRG_319:g.33720_33747delinsGAGCAAGACTCTGTCTCAGAAAAAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.291-291_291-264delinsGAGCAAGACTCTGTCTCAGAAAAAAAAA	ENSP00000490268.2:n.291-291_291-264delinsGAGCAAGACTCTGTCTCAGA...
ENST00000585748.3:c.-82-291_-82-264delinsGAGCAAGACTCTGTCTCAGAAAAAAAAA	ENSP00000477641.2:n.-82-291_-82-264delinsGAGCAAGACTCTGTCTCAGA...
ENST00000585851.2:c.291-2247_291-2220delinsGAGCAAGACTCTGTCTCAGAAAAAAAAA	ENSP00000467912.2:n.291-2247_291-2220delinsGAGCAAGACTCTGTCTCA...
ENST00000326873.12:c.291-291_291-264delinsGAGCAAGACTCTGTCTCAGAAAAAAAAA MANE Select	ENSP00000324856.6:n.291-291_291-264delinsGAGCAAGACTCTGTCTCAGA...
ENST00000652231.1:c.291-291_291-264delinsGAGCAAGACTCTGTCTCAGAAAAAAAAA	ENSP00000498804.1:n.291-291_291-264delinsGAGCAAGACTCTGTCTCAGA...
ENST00000326873.11:c.291-291_291-264delinsGAGCAAGACTCTGTCTCAGAAAAAAAAA	ENSP00000324856.6:n.291-291_291-264delinsGAGCAAGACTCTGTCTCAGA...
ENST00000585748.2:c.-82-291_-82-264delinsGAGCAAGACTCTGTCTCAGAAAAAAAAA	ENSP00000477641.1:n.-82-291_-82-264delinsGAGCAAGACTCTGTCTCAGA...
ENST00000585851.1:c.291-2247_291-2220delinsGAGCAAGACTCTGTCTCAGAAAAAAAAA	ENSP00000467912.1:n.291-2247_291-2220delinsGAGCAAGACTCTGTCTCA...
ENST00000586243.5:c.291-291_291-264delinsGAGCAAGACTCTGTCTCAGAAAAAAAAA	ENSP00000467240.2:n.291-291_291-264delinsGAGCAAGACTCTGTCTCAGA...
ENST00000586358.5:n.114-291_114-264delinsGAGCAAGACTCTGTCTCAGAAAAAAAAA
ENST00000589152.5:n.381-291_381-264delinsGAGCAAGACTCTGTCTCAGAAAAAAAAA
ENST00000593219.5:c.*116-291_*116-264delinsGAGCAAGACTCTGTCTCAGAAAAAAAAA	ENSP00000466610.1:n.*116-291_*116-264delinsGAGCAAGACTCTGTCTCA...
NM_000455.4:c.291-291_291-264delinsGAGCAAGACTCTGTCTCAGAAAAAAAAA , LRG_319t1:c.291-291_291-264delinsGAGCAAGACTCTGTCTCAGAAAAAAAAA	NP_000446.1:n.291-291_291-264delinsGAGCAAGACTCTGTCTCAGAAAAAAA...
XM_005259617.1:c.291-291_291-264delinsGAGCAAGACTCTGTCTCAGAAAAAAAAA	XP_005259674.1:n.291-291_291-264delinsGAGCAAGACTCTGTCTCAGAAAA...
XM_005259618.3:c.291-291_291-264delinsGAGCAAGACTCTGTCTCAGAAAAAAAAA	XP_005259675.1:n.291-291_291-264delinsGAGCAAGACTCTGTCTCAGAAAA...
XM_011528209.1:c.69-291_69-264delinsGAGCAAGACTCTGTCTCAGAAAAAAAAA	XP_011526511.1:n.69-291_69-264delinsGAGCAAGACTCTGTCTCAGAAAAAA...
XR_936204.1:n.916-291_916-264delinsGAGCAAGACTCTGTCTCAGAAAAAAAAA
XM_005259617.3:c.291-291_291-264delinsGAGCAAGACTCTGTCTCAGAAAAAAAAA	XP_005259674.1:n.291-291_291-264delinsGAGCAAGACTCTGTCTCAGAAAA...
XM_011528209.2:c.69-291_69-264delinsGAGCAAGACTCTGTCTCAGAAAAAAAAA	XP_011526511.1:n.69-291_69-264delinsGAGCAAGACTCTGTCTCAGAAAAAA...
XR_001753738.2:n.916-291_916-264delinsGAGCAAGACTCTGTCTCAGAAAAAAAAA
XR_001753739.1:n.916-291_916-264delinsGAGCAAGACTCTGTCTCAGAAAAAAAAA
XR_001753740.2:n.916-291_916-264delinsGAGCAAGACTCTGTCTCAGAAAAAAAAA
NM_000455.5:c.291-291_291-264delinsGAGCAAGACTCTGTCTCAGAAAAAAAAA MANE Select	NP_000446.1:n.291-291_291-264delinsGAGCAAGACTCTGTCTCAGAAAAAAA...