Canonical Allele Identifier: CA2499225341

Gene: STK11

Linked Data

• ClinVar Variation Id: 1073428
• ClinVar RCV Id: RCV001386418
• dbSNP Id: rs2145420792

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218480_1218488del , CM000681.2:g.1218480_1218488del	GRCh38
NC_000019.9:g.1218479_1218487del , CM000681.1:g.1218479_1218487del	GRCh37
NC_000019.8:g.1169479_1169487del	NCBI36
NG_007460.2:g.34074_34082del , LRG_319:g.34074_34082del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.354_362del	ENSP00000490268.2:p.Tyr118Ter
ENST00000585748.3:c.-19_-11del	ENSP00000477641.2:n.-19_-11del
ENST00000585851.2:c.291-1893_291-1885del	ENSP00000467912.2:n.291-1893_291-1885del
ENST00000326873.12:c.354_362del MANE Select	ENSP00000324856.6:p.Tyr118Ter
ENST00000652231.1:c.354_362del	ENSP00000498804.1:p.Tyr118Ter
ENST00000326873.11:c.354_362del	ENSP00000324856.6:p.Tyr118Ter
ENST00000585748.2:c.-19_-11del	ENSP00000477641.1:n.-19_-11del
ENST00000585851.1:c.291-1893_291-1885del	ENSP00000467912.1:n.291-1893_291-1885del
ENST00000586243.5:c.354_362del	ENSP00000467240.2:p.Tyr118Ter
ENST00000586358.5:n.177_185del
ENST00000589152.5:n.444_452del
ENST00000593219.5:c.*179_*187del	ENSP00000466610.1:n.*179_*187del
NM_000455.4:c.354_362del , LRG_319t1:c.354_362del	NP_000446.1:p.Tyr118Ter
XM_005259617.1:c.354_362del	XP_005259674.1:p.Tyr118Ter
XM_005259618.3:c.354_362del	XP_005259675.1:p.Tyr118Ter
XM_011528209.1:c.132_140del	XP_011526511.1:p.Tyr44Ter
XR_936204.1:n.979_987del
XM_005259617.3:c.354_362del	XP_005259674.1:p.Tyr118Ter
XM_011528209.2:c.132_140del	XP_011526511.1:p.Tyr44Ter
XR_001753738.2:n.979_987del
XR_001753739.1:n.979_987del
XR_001753740.2:n.979_987del
NM_000455.5:c.354_362del MANE Select	NP_000446.1:p.Tyr118Ter