Canonical Allele Identifier: CA402947967

Gene: STK11

Linked Data

• ClinVar Variation Id: 1801557
• ClinVar RCV Id: RCV003164590
• dbSNP Id: rs1555737480
• MyVariant Identifiers: chr19:g.1218501T>A (hg19) ; chr19:g.1218502T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218502T>A , CM000681.2:g.1218502T>A	GRCh38
NC_000019.9:g.1218501T>A , CM000681.1:g.1218501T>A	GRCh37
NC_000019.8:g.1169501T>A	NCBI36
NG_007460.2:g.34096T>A , LRG_319:g.34096T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.374+2T>A	ENSP00000490268.2:n.374+2T>A
ENST00000585748.3:c.2+2T>A	ENSP00000477641.2:n.2+2T>A
ENST00000585851.2:c.291-1871T>A	ENSP00000467912.2:n.291-1871T>A
ENST00000326873.12:c.374+2T>A MANE Select	ENSP00000324856.6:n.374+2T>A
ENST00000652231.1:c.374+2T>A	ENSP00000498804.1:n.374+2T>A
ENST00000326873.11:c.374+2T>A	ENSP00000324856.6:n.374+2T>A
ENST00000585748.2:c.2+2T>A	ENSP00000477641.1:n.2+2T>A
ENST00000585851.1:c.291-1871T>A	ENSP00000467912.1:n.291-1871T>A
ENST00000586243.5:c.374+2T>A	ENSP00000467240.2:n.374+2T>A
ENST00000586358.5:n.197+2T>A
ENST00000589152.5:n.464+2T>A
ENST00000593219.5:c.*199+2T>A	ENSP00000466610.1:n.*199+2T>A
NM_000455.4:c.374+2T>A , LRG_319t1:c.374+2T>A	NP_000446.1:n.374+2T>A
XM_005259617.1:c.374+2T>A	XP_005259674.1:n.374+2T>A
XM_005259618.3:c.374+2T>A	XP_005259675.1:n.374+2T>A
XM_011528209.1:c.152+2T>A	XP_011526511.1:n.152+2T>A
XR_936204.1:n.999+2T>A
XM_005259617.3:c.374+2T>A	XP_005259674.1:n.374+2T>A
XM_011528209.2:c.152+2T>A	XP_011526511.1:n.152+2T>A
XR_001753738.2:n.999+2T>A
XR_001753739.1:n.999+2T>A
XR_001753740.2:n.999+2T>A
NM_000455.5:c.374+2T>A MANE Select	NP_000446.1:n.374+2T>A