Canonical Allele Identifier: CA2573155766

Gene: STK11

Linked Data

• ClinVar Variation Id: 1647316
• ClinVar RCV Id: RCV002139038
• dbSNP Id: rs2145424937

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220568_1220572del , CM000681.2:g.1220568_1220572del	GRCh38
NC_000019.9:g.1220567_1220571del , CM000681.1:g.1220567_1220571del	GRCh37
NC_000019.8:g.1171567_1171571del	NCBI36
NG_007460.2:g.36162_36166del , LRG_319:g.36162_36166del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.598-13_598-9del	ENSP00000490268.2:n.598-13_598-9del
ENST00000585748.3:c.226-13_226-9del	ENSP00000477641.2:n.226-13_226-9del
ENST00000585851.2:c.424-13_424-9del	ENSP00000467912.2:n.424-13_424-9del
ENST00000326873.12:c.598-13_598-9del MANE Select	ENSP00000324856.6:n.598-13_598-9del
ENST00000652231.1:c.598-13_598-9del	ENSP00000498804.1:n.598-13_598-9del
ENST00000326873.11:c.598-13_598-9del	ENSP00000324856.6:n.598-13_598-9del
ENST00000585851.1:c.424-13_424-9del	ENSP00000467912.1:n.424-13_424-9del
ENST00000586243.5:c.598-13_598-9del	ENSP00000467240.2:n.598-13_598-9del
ENST00000586358.5:n.483_487del
ENST00000589152.5:n.688-13_688-9del
ENST00000591133.2:n.556_560del
NM_000455.4:c.598-13_598-9del , LRG_319t1:c.598-13_598-9del	NP_000446.1:n.598-13_598-9del
XM_005259617.1:c.598-13_598-9del	XP_005259674.1:n.598-13_598-9del
XM_005259618.3:c.598-13_598-9del	XP_005259675.1:n.598-13_598-9del
XM_011528209.1:c.376-13_376-9del	XP_011526511.1:n.376-13_376-9del
XR_936204.1:n.1223-13_1223-9del
XM_005259617.3:c.598-13_598-9del	XP_005259674.1:n.598-13_598-9del
XM_011528209.2:c.376-13_376-9del	XP_011526511.1:n.376-13_376-9del
XR_001753738.2:n.1223-13_1223-9del
XR_001753739.1:n.1223-13_1223-9del
XR_001753740.2:n.1223-13_1223-9del
NM_000455.5:c.598-13_598-9del MANE Select	NP_000446.1:n.598-13_598-9del