Canonical Allele Identifier: CA2499225357

Gene: STK11

Linked Data

• ClinVar Variation Id: 1082086
• ClinVar RCV Id: RCV001398259
• dbSNP Id: rs2145435780

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226451del , CM000681.2:g.1226451del	GRCh38
NC_000019.9:g.1226450del , CM000681.1:g.1226450del	GRCh37
NC_000019.8:g.1177450del	NCBI36
NG_007460.2:g.42045del , LRG_319:g.42045del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2707del	ENSP00000490268.2:n.*2707del
ENST00000585748.3:c.737-3del	ENSP00000477641.2:n.737-3del
ENST00000585851.2:c.935-3del	ENSP00000467912.2:n.935-3del
ENST00000326873.12:c.1109-3del MANE Select	ENSP00000324856.6:n.1109-3del
ENST00000326873.11:c.1109-3del	ENSP00000324856.6:n.1109-3del
ENST00000585465.2:n.2839del
ENST00000586243.5:c.1109-3del	ENSP00000467240.2:n.1109-3del
ENST00000589152.5:n.1807-3del
NM_000455.4:c.1109-3del , LRG_319t1:c.1109-3del	NP_000446.1:n.1109-3del
XM_005259617.1:c.1109-8del	XP_005259674.1:n.1109-8del
XM_011528209.1:c.887-8del	XP_011526511.1:n.887-8del
XM_005259617.3:c.1109-8del	XP_005259674.1:n.1109-8del
XM_011528209.2:c.887-8del	XP_011526511.1:n.887-8del
XR_001753738.2:n.1915-3del
XR_001753740.2:n.1885-3del
NM_000455.5:c.1109-3del MANE Select	NP_000446.1:n.1109-3del