Canonical Allele Identifier: CA045239

Gene: STK11

Linked Data

• ClinVar Variation Id: 384195
• ClinVar RCV Id: RCV000441838 ; RCV002065080
• dbSNP Id: rs770723400
• ExAC: 19:1223187 G / A
• gnomAD v2: 19-1223187-G-A
• gnomAD v3: 19-1223188-G-A
• gnomAD v4: 19-1223188-G-A
• MyVariant Identifiers: chr19:g.1223187G>A (hg19) ; chr19:g.1223188G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1223188G>A , CM000681.2:g.1223188G>A	GRCh38
NC_000019.9:g.1223187G>A , CM000681.1:g.1223187G>A	GRCh37
NC_000019.8:g.1174187G>A	NCBI36
NG_007460.2:g.38782G>A , LRG_319:g.38782G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.1108+16G>A	ENSP00000490268.2:n.1108+16G>A
ENST00000585748.3:c.736+16G>A	ENSP00000477641.2:n.736+16G>A
ENST00000585851.2:c.934+16G>A	ENSP00000467912.2:n.934+16G>A
ENST00000326873.12:c.1108+16G>A MANE Select	ENSP00000324856.6:n.1108+16G>A
ENST00000652231.1:c.1108+16G>A	ENSP00000498804.1:n.1108+16G>A
ENST00000326873.11:c.1108+16G>A	ENSP00000324856.6:n.1108+16G>A
ENST00000585465.2:n.25+16G>A
ENST00000586243.5:c.1108+16G>A	ENSP00000467240.2:n.1108+16G>A
ENST00000589152.5:n.1806+16G>A
NM_000455.4:c.1108+16G>A , LRG_319t1:c.1108+16G>A	NP_000446.1:n.1108+16G>A
XM_005259617.1:c.1108+16G>A	XP_005259674.1:n.1108+16G>A
XM_005259618.3:c.1108+16G>A	XP_005259675.1:n.1108+16G>A
XM_011528209.1:c.886+16G>A	XP_011526511.1:n.886+16G>A
XR_936204.1:n.1884+16G>A
XM_005259617.3:c.1108+16G>A	XP_005259674.1:n.1108+16G>A
XM_011528209.2:c.886+16G>A	XP_011526511.1:n.886+16G>A
XR_001753738.2:n.1914+16G>A
XR_001753739.1:n.1914+16G>A
XR_001753740.2:n.1884+16G>A
NM_000455.5:c.1108+16G>A MANE Select	NP_000446.1:n.1108+16G>A