Canonical Allele Identifier: CA10577590

Gene: STK11

Linked Data

• ClinVar Variation Id: 234549
• ClinVar RCV Id: RCV000221102 ; RCV001046088 ; RCV001016064 ; RCV002485442
• dbSNP Id: rs876661079
• gnomAD v4: 19-1206938-C-G
• MyVariant Identifiers: chr19:g.1206937C>G (hg19) ; chr19:g.1206938C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1206938C>G , CM000681.2:g.1206938C>G	GRCh38
NC_000019.9:g.1206937C>G , CM000681.1:g.1206937C>G	GRCh37
NC_000019.8:g.1157937C>G	NCBI36
NG_007460.2:g.22532C>G , LRG_319:g.22532C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.25C>G	ENSP00000490268.2:p.Leu9Val
ENST00000585748.3:c.-82-11479C>G	ENSP00000477641.2:n.-82-11479C>G
ENST00000585851.2:c.25C>G	ENSP00000467912.2:p.Leu9Val
ENST00000326873.12:c.25C>G MANE Select	ENSP00000324856.6:p.Leu9Val
ENST00000652231.1:c.25C>G	ENSP00000498804.1:p.Leu9Val
ENST00000326873.11:c.25C>G	ENSP00000324856.6:p.Leu9Val
ENST00000585748.2:c.-82-11479C>G	ENSP00000477641.1:n.-82-11479C>G
ENST00000585851.1:c.25C>G	ENSP00000467912.1:p.Leu9Val
ENST00000586243.5:c.25C>G	ENSP00000467240.2:p.Leu9Val
ENST00000589152.5:n.115C>G
ENST00000593219.5:c.25C>G	ENSP00000466610.1:p.Leu9Val
NM_000455.4:c.25C>G , LRG_319t1:c.25C>G	NP_000446.1:p.Leu9Val
XM_005259617.1:c.25C>G	XP_005259674.1:p.Leu9Val
XM_005259618.3:c.25C>G	XP_005259675.1:p.Leu9Val
XM_011528209.1:c.-329C>G	XP_011526511.1:n.-329C>G
XR_936204.1:n.650C>G
XM_005259617.3:c.25C>G	XP_005259674.1:p.Leu9Val
XM_011528209.2:c.-329C>G	XP_011526511.1:n.-329C>G
XR_001753738.2:n.650C>G
XR_001753739.1:n.650C>G
XR_001753740.2:n.650C>G
NM_000455.5:c.25C>G MANE Select	NP_000446.1:p.Leu9Val