Canonical Allele Identifier: CA2499225355

Gene: STK11

Linked Data

• ClinVar Variation Id: 1068953
• ClinVar RCV Id: RCV001380657
• dbSNP Id: rs2145431039

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1223088_1223091del , CM000681.2:g.1223088_1223091del	GRCh38
NC_000019.9:g.1223087_1223090del , CM000681.1:g.1223087_1223090del	GRCh37
NC_000019.8:g.1174087_1174090del	NCBI36
NG_007460.2:g.38682_38685del , LRG_319:g.38682_38685del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.1024_1027del	ENSP00000490268.2:p.Glu342ThrfsTer?
ENST00000585748.3:c.652_655del	ENSP00000477641.2:p.Glu218ThrfsTer?
ENST00000585851.2:c.850_853del	ENSP00000467912.2:p.Glu284ThrfsTer?
ENST00000326873.12:c.1024_1027del MANE Select	ENSP00000324856.6:p.Glu342ThrfsTer?
ENST00000652231.1:c.1024_1027del	ENSP00000498804.1:p.Glu342ThrfsTer?
ENST00000326873.11:c.1024_1027del	ENSP00000324856.6:p.Glu342ThrfsTer?
ENST00000586243.5:c.1024_1027del	ENSP00000467240.2:p.Glu342ThrfsTer?
ENST00000589152.5:n.1722_1725del
ENST00000591133.2:n.995_998del
NM_000455.4:c.1024_1027del , LRG_319t1:c.1024_1027del	NP_000446.1:p.Glu342ThrfsTer?
XM_005259617.1:c.1024_1027del	XP_005259674.1:p.Glu342ThrfsTer?
XM_005259618.3:c.1024_1027del	XP_005259675.1:p.Glu342ThrfsTer?
XM_011528209.1:c.802_805del	XP_011526511.1:p.Glu268ThrfsTer?
XR_936204.1:n.1800_1803del
XM_005259617.3:c.1024_1027del	XP_005259674.1:p.Glu342ThrfsTer?
XM_011528209.2:c.802_805del	XP_011526511.1:p.Glu268ThrfsTer?
XR_001753738.2:n.1830_1833del
XR_001753739.1:n.1830_1833del
XR_001753740.2:n.1800_1803del
NM_000455.5:c.1024_1027del MANE Select	NP_000446.1:p.Glu342ThrfsTer?