Canonical Allele Identifier: CA2735570466

Gene: STK11

Linked Data

• dbSNP Id: rs2145422170

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219331del , CM000681.2:g.1219331del	GRCh38
NC_000019.9:g.1219330del , CM000681.1:g.1219330del	GRCh37
NC_000019.8:g.1170330del	NCBI36
NG_007460.2:g.34925del , LRG_319:g.34925del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.382del	ENSP00000490268.2:p.Val128Ter
ENST00000585748.3:c.10del	ENSP00000477641.2:p.Val4Ter
ENST00000585851.2:c.291-1042del	ENSP00000467912.2:n.291-1042del
ENST00000326873.12:c.382del MANE Select	ENSP00000324856.6:p.Val128Ter
ENST00000652231.1:c.382del	ENSP00000498804.1:p.Val128Ter
ENST00000326873.11:c.382del	ENSP00000324856.6:p.Val128Ter
ENST00000585748.2:c.10del	ENSP00000477641.1:p.Val4Ter
ENST00000585851.1:c.291-1042del	ENSP00000467912.1:n.291-1042del
ENST00000586243.5:c.382del	ENSP00000467240.2:p.Val128Ter
ENST00000586358.5:n.205del
ENST00000589152.5:n.472del
ENST00000593219.5:c.*207del	ENSP00000466610.1:n.*207del
NM_000455.4:c.382del , LRG_319t1:c.382del	NP_000446.1:p.Val128Ter
XM_005259617.1:c.382del	XP_005259674.1:p.Val128Ter
XM_005259618.3:c.382del	XP_005259675.1:p.Val128Ter
XM_011528209.1:c.160del	XP_011526511.1:p.Val54Ter
XR_936204.1:n.1007del
XM_005259617.3:c.382del	XP_005259674.1:p.Val128Ter
XM_011528209.2:c.160del	XP_011526511.1:p.Val54Ter
XR_001753738.2:n.1007del
XR_001753739.1:n.1007del
XR_001753740.2:n.1007del
NM_000455.5:c.382del MANE Select	NP_000446.1:p.Val128Ter