Canonical Allele Identifier: CA402954159

Gene: STK11

Linked Data

• ClinVar Variation Id: 1391364
• ClinVar RCV Id: RCV001893040
• dbSNP Id: rs2145436527
• MyVariant Identifiers: chr19:g.1226614A>G (hg19) ; chr19:g.1226615A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226615A>G , CM000681.2:g.1226615A>G	GRCh38
NC_000019.9:g.1226614A>G , CM000681.1:g.1226614A>G	GRCh37
NC_000019.8:g.1177614A>G	NCBI36
NG_007460.2:g.42209A>G , LRG_319:g.42209A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2871A>G	ENSP00000490268.2:n.*2871A>G
ENST00000585748.3:c.898A>G	ENSP00000477641.2:p.Ile300Val
ENST00000585851.2:c.1096A>G	ENSP00000467912.2:p.Ile366Val
ENST00000326873.12:c.1270A>G MANE Select	ENSP00000324856.6:p.Ile424Val
ENST00000326873.11:c.1270A>G	ENSP00000324856.6:p.Ile424Val
ENST00000585465.2:n.3003A>G
ENST00000586243.5:c.1267A>G	ENSP00000467240.2:p.Ile423Val
ENST00000589152.5:n.1968A>G
NM_000455.4:c.1270A>G , LRG_319t1:c.1270A>G	NP_000446.1:p.Ile424Val
XM_005259617.1:c.1265A>G	XP_005259674.1:p.Asp422Gly
XM_011528209.1:c.1043A>G	XP_011526511.1:p.Asp348Gly
XM_005259617.3:c.1265A>G	XP_005259674.1:p.Asp422Gly
XM_011528209.2:c.1043A>G	XP_011526511.1:p.Asp348Gly
XR_001753738.2:n.2076A>G
XR_001753740.2:n.2046A>G
NM_000455.5:c.1270A>G MANE Select	NP_000446.1:p.Ile424Val