Canonical Allele Identifier: CA402951899

Gene: STK11

Linked Data

• ClinVar Variation Id: 527832
• ClinVar RCV Id: RCV000632830 ; RCV001175695
• dbSNP Id: rs1555739334
• MyVariant Identifiers: chr19:g.1223141A>G (hg19) ; chr19:g.1223142A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1223142A>G , CM000681.2:g.1223142A>G	GRCh38
NC_000019.9:g.1223141A>G , CM000681.1:g.1223141A>G	GRCh37
NC_000019.8:g.1174141A>G	NCBI36
NG_007460.2:g.38736A>G , LRG_319:g.38736A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.1078A>G	ENSP00000490268.2:p.Ile360Val
ENST00000585748.3:c.706A>G	ENSP00000477641.2:p.Ile236Val
ENST00000585851.2:c.904A>G	ENSP00000467912.2:p.Ile302Val
ENST00000326873.12:c.1078A>G MANE Select	ENSP00000324856.6:p.Ile360Val
ENST00000652231.1:c.1078A>G	ENSP00000498804.1:p.Ile360Val
ENST00000326873.11:c.1078A>G	ENSP00000324856.6:p.Ile360Val
ENST00000586243.5:c.1078A>G	ENSP00000467240.2:p.Ile360Val
ENST00000589152.5:n.1776A>G
NM_000455.4:c.1078A>G , LRG_319t1:c.1078A>G	NP_000446.1:p.Ile360Val
XM_005259617.1:c.1078A>G	XP_005259674.1:p.Ile360Val
XM_005259618.3:c.1078A>G	XP_005259675.1:p.Ile360Val
XM_011528209.1:c.856A>G	XP_011526511.1:p.Ile286Val
XR_936204.1:n.1854A>G
XM_005259617.3:c.1078A>G	XP_005259674.1:p.Ile360Val
XM_011528209.2:c.856A>G	XP_011526511.1:p.Ile286Val
XR_001753738.2:n.1884A>G
XR_001753739.1:n.1884A>G
XR_001753740.2:n.1854A>G
NM_000455.5:c.1078A>G MANE Select	NP_000446.1:p.Ile360Val