Canonical Allele Identifier: CA2582596941

Gene: STK11

Linked Data

• gnomAD v4: 19-1226134-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226134_1226135insC , CM000681.2:g.1226134_1226135insC	GRCh38
NC_000019.9:g.1226133_1226134insC , CM000681.1:g.1226133_1226134insC	GRCh37
NC_000019.8:g.1177133_1177134insC	NCBI36
NG_007460.2:g.41728_41729insC , LRG_319:g.41728_41729insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2390_*2391insC	ENSP00000490268.2:n.*2390_*2391insC
ENST00000585748.3:c.737-320_737-319insC	ENSP00000477641.2:n.737-320_737-319insC
ENST00000585851.2:c.935-320_935-319insC	ENSP00000467912.2:n.935-320_935-319insC
ENST00000326873.12:c.1109-320_1109-319insC MANE Select	ENSP00000324856.6:n.1109-320_1109-319insC
ENST00000326873.11:c.1109-320_1109-319insC	ENSP00000324856.6:n.1109-320_1109-319insC
ENST00000585465.2:n.2522_2523insC
ENST00000586243.5:c.1109-320_1109-319insC	ENSP00000467240.2:n.1109-320_1109-319insC
ENST00000589152.5:n.1807-320_1807-319insC
NM_000455.4:c.1109-320_1109-319insC , LRG_319t1:c.1109-320_1109-319insC	NP_000446.1:n.1109-320_1109-319insC
XM_005259617.1:c.1109-325_1109-324insC	XP_005259674.1:n.1109-325_1109-324insC
XM_011528209.1:c.887-325_887-324insC	XP_011526511.1:n.887-325_887-324insC
XM_005259617.3:c.1109-325_1109-324insC	XP_005259674.1:n.1109-325_1109-324insC
XM_011528209.2:c.887-325_887-324insC	XP_011526511.1:n.887-325_887-324insC
XR_001753738.2:n.1915-320_1915-319insC
XR_001753740.2:n.1885-320_1885-319insC
NM_000455.5:c.1109-320_1109-319insC MANE Select	NP_000446.1:n.1109-320_1109-319insC