Canonical Allele Identifier: CA402948801

Gene: STK11

Linked Data

• ClinVar Variation Id: 571305
• ClinVar RCV Id: RCV000692416
• dbSNP Id: rs1568707502
• COSMIC: COSM5991519
• MyVariant Identifiers: chr19:g.1220380G>A (hg19) ; chr19:g.1220381G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220381G>A , CM000681.2:g.1220381G>A	GRCh38
NC_000019.9:g.1220380G>A , CM000681.1:g.1220380G>A	GRCh37
NC_000019.8:g.1171380G>A	NCBI36
NG_007460.2:g.35975G>A , LRG_319:g.35975G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.473G>A	ENSP00000490268.2:p.Cys158Tyr
ENST00000585748.3:c.101G>A	ENSP00000477641.2:p.Cys34Tyr
ENST00000585851.2:c.299G>A	ENSP00000467912.2:p.Cys100Tyr
ENST00000326873.12:c.473G>A MANE Select	ENSP00000324856.6:p.Cys158Tyr
ENST00000652231.1:c.473G>A	ENSP00000498804.1:p.Cys158Tyr
ENST00000326873.11:c.473G>A	ENSP00000324856.6:p.Cys158Tyr
ENST00000585851.1:c.299G>A	ENSP00000467912.1:p.Cys100Tyr
ENST00000586243.5:c.473G>A	ENSP00000467240.2:p.Cys158Tyr
ENST00000586358.5:n.296G>A
ENST00000589152.5:n.563G>A
ENST00000591133.2:n.369G>A
NM_000455.4:c.473G>A , LRG_319t1:c.473G>A	NP_000446.1:p.Cys158Tyr
XM_005259617.1:c.473G>A	XP_005259674.1:p.Cys158Tyr
XM_005259618.3:c.473G>A	XP_005259675.1:p.Cys158Tyr
XM_011528209.1:c.251G>A	XP_011526511.1:p.Cys84Tyr
XR_936204.1:n.1098G>A
XM_005259617.3:c.473G>A	XP_005259674.1:p.Cys158Tyr
XM_011528209.2:c.251G>A	XP_011526511.1:p.Cys84Tyr
XR_001753738.2:n.1098G>A
XR_001753739.1:n.1098G>A
XR_001753740.2:n.1098G>A
NM_000455.5:c.473G>A MANE Select	NP_000446.1:p.Cys158Tyr