Canonical Allele Identifier: CA402950551

Gene: STK11

Linked Data

• ClinVar Variation Id: 568685
• ClinVar RCV Id: RCV003459677
• dbSNP Id: rs1568709259
• gnomAD v4: 19-1221277-A-G
• MyVariant Identifiers: chr19:g.1221276A>G (hg19) ; chr19:g.1221277A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1221277A>G , CM000681.2:g.1221277A>G	GRCh38
NC_000019.9:g.1221276A>G , CM000681.1:g.1221276A>G	GRCh37
NC_000019.8:g.1172276A>G	NCBI36
NG_007460.2:g.36871A>G , LRG_319:g.36871A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.799A>G	ENSP00000490268.2:p.Ile267Val
ENST00000585748.3:c.427A>G	ENSP00000477641.2:p.Ile143Val
ENST00000585851.2:c.625A>G	ENSP00000467912.2:p.Ile209Val
ENST00000326873.12:c.799A>G MANE Select	ENSP00000324856.6:p.Ile267Val
ENST00000652231.1:c.799A>G	ENSP00000498804.1:p.Ile267Val
ENST00000326873.11:c.799A>G	ENSP00000324856.6:p.Ile267Val
ENST00000586243.5:c.799A>G	ENSP00000467240.2:p.Ile267Val
ENST00000586358.5:n.697A>G
ENST00000589152.5:n.889A>G
ENST00000591133.2:n.770A>G
NM_000455.4:c.799A>G , LRG_319t1:c.799A>G	NP_000446.1:p.Ile267Val
XM_005259617.1:c.799A>G	XP_005259674.1:p.Ile267Val
XM_005259618.3:c.799A>G	XP_005259675.1:p.Ile267Val
XM_011528209.1:c.577A>G	XP_011526511.1:p.Ile193Val
XR_936204.1:n.1424A>G
XM_005259617.3:c.799A>G	XP_005259674.1:p.Ile267Val
XM_011528209.2:c.577A>G	XP_011526511.1:p.Ile193Val
XR_001753738.2:n.1424A>G
XR_001753739.1:n.1424A>G
XR_001753740.2:n.1424A>G
NM_000455.5:c.799A>G MANE Select	NP_000446.1:p.Ile267Val