Canonical Allele Identifier: CA2573155759

Gene: STK11

Linked Data

• ClinVar Variation Id: 1503175
• ClinVar RCV Id: RCV002022693
• dbSNP Id: rs2145424107

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220374_1220385del , CM000681.2:g.1220374_1220385del	GRCh38
NC_000019.9:g.1220373_1220384del , CM000681.1:g.1220373_1220384del	GRCh37
NC_000019.8:g.1171373_1171384del	NCBI36
NG_007460.2:g.35968_35979del , LRG_319:g.35968_35979del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.466_477del	ENSP00000490268.2:p.Tyr156_Gln159del
ENST00000585748.3:c.94_105del	ENSP00000477641.2:p.Tyr32_Gln35del
ENST00000585851.2:c.292_303del	ENSP00000467912.2:p.Tyr98_Gln101del
ENST00000326873.12:c.466_477del MANE Select	ENSP00000324856.6:p.Tyr156_Gln159del
ENST00000652231.1:c.466_477del	ENSP00000498804.1:p.Tyr156_Gln159del
ENST00000326873.11:c.466_477del	ENSP00000324856.6:p.Tyr156_Gln159del
ENST00000585851.1:c.292_303del	ENSP00000467912.1:p.Tyr98_Gln101del
ENST00000586243.5:c.466_477del	ENSP00000467240.2:p.Tyr156_Gln159del
ENST00000586358.5:n.289_300del
ENST00000589152.5:n.556_567del
ENST00000591133.2:n.362_373del
NM_000455.4:c.466_477del , LRG_319t1:c.466_477del	NP_000446.1:p.Tyr156_Gln159del
XM_005259617.1:c.466_477del	XP_005259674.1:p.Tyr156_Gln159del
XM_005259618.3:c.466_477del	XP_005259675.1:p.Tyr156_Gln159del
XM_011528209.1:c.244_255del	XP_011526511.1:p.Tyr82_Gln85del
XR_936204.1:n.1091_1102del
XM_005259617.3:c.466_477del	XP_005259674.1:p.Tyr156_Gln159del
XM_011528209.2:c.244_255del	XP_011526511.1:p.Tyr82_Gln85del
XR_001753738.2:n.1091_1102del
XR_001753739.1:n.1091_1102del
XR_001753740.2:n.1091_1102del
NM_000455.5:c.466_477del MANE Select	NP_000446.1:p.Tyr156_Gln159del