Canonical Allele Identifier: CA402953680

Gene: STK11

Linked Data

• ClinVar Variation Id: 1026241
• ClinVar RCV Id: RCV001326665 ; RCV002350607
• dbSNP Id: rs2080822902
• gnomAD v4: 19-1226546-A-G
• MyVariant Identifiers: chr19:g.1226545A>G (hg19) ; chr19:g.1226546A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226546A>G , CM000681.2:g.1226546A>G	GRCh38
NC_000019.9:g.1226545A>G , CM000681.1:g.1226545A>G	GRCh37
NC_000019.8:g.1177545A>G	NCBI36
NG_007460.2:g.42140A>G , LRG_319:g.42140A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2802A>G	ENSP00000490268.2:n.*2802A>G
ENST00000585748.3:c.829A>G	ENSP00000477641.2:p.Ser277Gly
ENST00000585851.2:c.1027A>G	ENSP00000467912.2:p.Ser343Gly
ENST00000326873.12:c.1201A>G MANE Select	ENSP00000324856.6:p.Ser401Gly
ENST00000326873.11:c.1201A>G	ENSP00000324856.6:p.Ser401Gly
ENST00000585465.2:n.2934A>G
ENST00000586243.5:c.1201A>G	ENSP00000467240.2:p.Ser401Gly
ENST00000589152.5:n.1899A>G
NM_000455.4:c.1201A>G , LRG_319t1:c.1201A>G	NP_000446.1:p.Ser401Gly
XM_005259617.1:c.1196A>G	XP_005259674.1:p.Glu399Gly
XM_011528209.1:c.974A>G	XP_011526511.1:p.Glu325Gly
XM_005259617.3:c.1196A>G	XP_005259674.1:p.Glu399Gly
XM_011528209.2:c.974A>G	XP_011526511.1:p.Glu325Gly
XR_001753738.2:n.2007A>G
XR_001753740.2:n.1977A>G
NM_000455.5:c.1201A>G MANE Select	NP_000446.1:p.Ser401Gly