Canonical Allele Identifier: CA402947962

Gene: STK11

Linked Data

• ClinVar Variation Id: 428788
• ClinVar RCV Id: RCV000492655 ; RCV001214909
• dbSNP Id: rs1131690951
• MyVariant Identifiers: chr19:g.1218500A>G (hg19) ; chr19:g.1218501A>G (hg38)
• PubMed: PMID:12112668 ; PMID:15608654 ; PMID:16287113 ; PMID:17404884

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218501A>G , CM000681.2:g.1218501A>G	GRCh38
NC_000019.9:g.1218500A>G , CM000681.1:g.1218500A>G	GRCh37
NC_000019.8:g.1169500A>G	NCBI36
NG_007460.2:g.34095A>G , LRG_319:g.34095A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.374+1A>G	ENSP00000490268.2:n.374+1A>G
ENST00000585748.3:c.2+1A>G	ENSP00000477641.2:n.2+1A>G
ENST00000585851.2:c.291-1872A>G	ENSP00000467912.2:n.291-1872A>G
ENST00000326873.12:c.374+1A>G MANE Select	ENSP00000324856.6:n.374+1A>G
ENST00000652231.1:c.374+1A>G	ENSP00000498804.1:n.374+1A>G
ENST00000326873.11:c.374+1A>G	ENSP00000324856.6:n.374+1A>G
ENST00000585748.2:c.2+1A>G	ENSP00000477641.1:n.2+1A>G
ENST00000585851.1:c.291-1872A>G	ENSP00000467912.1:n.291-1872A>G
ENST00000586243.5:c.374+1A>G	ENSP00000467240.2:n.374+1A>G
ENST00000586358.5:n.197+1A>G
ENST00000589152.5:n.464+1A>G
ENST00000593219.5:c.*199+1A>G	ENSP00000466610.1:n.*199+1A>G
NM_000455.4:c.374+1A>G , LRG_319t1:c.374+1A>G	NP_000446.1:n.374+1A>G
XM_005259617.1:c.374+1A>G	XP_005259674.1:n.374+1A>G
XM_005259618.3:c.374+1A>G	XP_005259675.1:n.374+1A>G
XM_011528209.1:c.152+1A>G	XP_011526511.1:n.152+1A>G
XR_936204.1:n.999+1A>G
XM_005259617.3:c.374+1A>G	XP_005259674.1:n.374+1A>G
XM_011528209.2:c.152+1A>G	XP_011526511.1:n.152+1A>G
XR_001753738.2:n.999+1A>G
XR_001753739.1:n.999+1A>G
XR_001753740.2:n.999+1A>G
NM_000455.5:c.374+1A>G MANE Select	NP_000446.1:n.374+1A>G