Canonical Allele Identifier: CA402943031

Gene: STK11

Linked Data

• ClinVar Variation Id: 651673
• ClinVar RCV Id: RCV000807083
• dbSNP Id: rs1360284524
• MyVariant Identifiers: chr19:g.1206928C>A (hg19) ; chr19:g.1206929C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1206929C>A , CM000681.2:g.1206929C>A	GRCh38
NC_000019.9:g.1206928C>A , CM000681.1:g.1206928C>A	GRCh37
NC_000019.8:g.1157928C>A	NCBI36
NG_007460.2:g.22523C>A , LRG_319:g.22523C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.16C>A	ENSP00000490268.2:p.Pro6Thr
ENST00000585748.3:c.-82-11488C>A	ENSP00000477641.2:n.-82-11488C>A
ENST00000585851.2:c.16C>A	ENSP00000467912.2:p.Pro6Thr
ENST00000326873.12:c.16C>A MANE Select	ENSP00000324856.6:p.Pro6Thr
ENST00000652231.1:c.16C>A	ENSP00000498804.1:p.Pro6Thr
ENST00000326873.11:c.16C>A	ENSP00000324856.6:p.Pro6Thr
ENST00000585748.2:c.-82-11488C>A	ENSP00000477641.1:n.-82-11488C>A
ENST00000585851.1:c.16C>A	ENSP00000467912.1:p.Pro6Thr
ENST00000586243.5:c.16C>A	ENSP00000467240.2:p.Pro6Thr
ENST00000589152.5:n.106C>A
ENST00000593219.5:c.16C>A	ENSP00000466610.1:p.Pro6Thr
NM_000455.4:c.16C>A , LRG_319t1:c.16C>A	NP_000446.1:p.Pro6Thr
XM_005259617.1:c.16C>A	XP_005259674.1:p.Pro6Thr
XM_005259618.3:c.16C>A	XP_005259675.1:p.Pro6Thr
XM_011528209.1:c.-338C>A	XP_011526511.1:n.-338C>A
XR_936204.1:n.641C>A
XM_005259617.3:c.16C>A	XP_005259674.1:p.Pro6Thr
XM_011528209.2:c.-338C>A	XP_011526511.1:n.-338C>A
XR_001753738.2:n.641C>A
XR_001753739.1:n.641C>A
XR_001753740.2:n.641C>A
NM_000455.5:c.16C>A MANE Select	NP_000446.1:p.Pro6Thr