Canonical Allele Identifier: CA023243

Gene: STK11

Linked Data

• ClinVar Variation Id: 182902
• ClinVar RCV Id: RCV000160995 ; RCV000763422 ; RCV001041130
• dbSNP Id: rs730881976
• MyVariant Identifiers: chr19:g.1220701C>G (hg19) ; chr19:g.1220702C>G (hg38)
• PubMed: PMID:23399955

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220702C>G , CM000681.2:g.1220702C>G	GRCh38
NC_000019.9:g.1220701C>G , CM000681.1:g.1220701C>G	GRCh37
NC_000019.8:g.1171701C>G	NCBI36
NG_007460.2:g.36296C>G , LRG_319:g.36296C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.719C>G	ENSP00000490268.2:p.Ser240Trp
ENST00000585748.3:c.347C>G	ENSP00000477641.2:p.Ser116Trp
ENST00000585851.2:c.545C>G	ENSP00000467912.2:p.Ser182Trp
ENST00000326873.12:c.719C>G MANE Select	ENSP00000324856.6:p.Ser240Trp
ENST00000652231.1:c.719C>G	ENSP00000498804.1:p.Ser240Trp
ENST00000326873.11:c.719C>G	ENSP00000324856.6:p.Ser240Trp
ENST00000586243.5:c.719C>G	ENSP00000467240.2:p.Ser240Trp
ENST00000586358.5:n.617C>G
ENST00000589152.5:n.809C>G
ENST00000591133.2:n.690C>G
NM_000455.4:c.719C>G , LRG_319t1:c.719C>G	NP_000446.1:p.Ser240Trp
XM_005259617.1:c.719C>G	XP_005259674.1:p.Ser240Trp
XM_005259618.3:c.719C>G	XP_005259675.1:p.Ser240Trp
XM_011528209.1:c.497C>G	XP_011526511.1:p.Ser166Trp
XR_936204.1:n.1344C>G
XM_005259617.3:c.719C>G	XP_005259674.1:p.Ser240Trp
XM_011528209.2:c.497C>G	XP_011526511.1:p.Ser166Trp
XR_001753738.2:n.1344C>G
XR_001753739.1:n.1344C>G
XR_001753740.2:n.1344C>G
NM_000455.5:c.719C>G MANE Select	NP_000446.1:p.Ser240Trp