Canonical Allele Identifier: CA2580096033

Gene: STK11

Linked Data

• ClinVar Variation Id: 2016738
• ClinVar RCV Id: RCV002844047

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219334del , CM000681.2:g.1219334del	GRCh38
NC_000019.9:g.1219333del , CM000681.1:g.1219333del	GRCh37
NC_000019.8:g.1170333del	NCBI36
NG_007460.2:g.34928del , LRG_319:g.34928del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.385del	ENSP00000490268.2:p.Met129TrpfsTer?
ENST00000585748.3:c.13del	ENSP00000477641.2:p.Met5TrpfsTer?
ENST00000585851.2:c.291-1039del	ENSP00000467912.2:n.291-1039del
ENST00000326873.12:c.385del MANE Select	ENSP00000324856.6:p.Met129TrpfsTer?
ENST00000652231.1:c.385del	ENSP00000498804.1:p.Met129TrpfsTer?
ENST00000326873.11:c.385del	ENSP00000324856.6:p.Met129TrpfsTer?
ENST00000585748.2:c.13del	ENSP00000477641.1:p.Met5TrpfsTer?
ENST00000585851.1:c.291-1039del	ENSP00000467912.1:n.291-1039del
ENST00000586243.5:c.385del	ENSP00000467240.2:p.Met129TrpfsTer?
ENST00000586358.5:n.208del
ENST00000589152.5:n.475del
ENST00000593219.5:c.*210del	ENSP00000466610.1:n.*210del
NM_000455.4:c.385del , LRG_319t1:c.385del	NP_000446.1:p.Met129TrpfsTer?
XM_005259617.1:c.385del	XP_005259674.1:p.Met129TrpfsTer?
XM_005259618.3:c.385del	XP_005259675.1:p.Met129TrpfsTer?
XM_011528209.1:c.163del	XP_011526511.1:p.Met55TrpfsTer?
XR_936204.1:n.1010del
XM_005259617.3:c.385del	XP_005259674.1:p.Met129TrpfsTer?
XM_011528209.2:c.163del	XP_011526511.1:p.Met55TrpfsTer?
XR_001753738.2:n.1010del
XR_001753739.1:n.1010del
XR_001753740.2:n.1010del
NM_000455.5:c.385del MANE Select	NP_000446.1:p.Met129TrpfsTer?