Canonical Allele Identifier: CA047373

Gene: STK11

Linked Data

• ClinVar Variation Id: 215737
• ClinVar RCV Id: RCV000434543 ; RCV000990126 ; RCV001188671 ; RCV001284241 ; RCV003907746
• dbSNP Id: rs762297795
• ExAC: 19:1218508 T / A
• gnomAD v2: 19-1218508-T-A
• gnomAD v3: 19-1218509-T-A
• gnomAD v4: 19-1218509-T-A
• MyVariant Identifiers: chr19:g.1218508T>A (hg19) ; chr19:g.1218509T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218509T>A , CM000681.2:g.1218509T>A	GRCh38
NC_000019.9:g.1218508T>A , CM000681.1:g.1218508T>A	GRCh37
NC_000019.8:g.1169508T>A	NCBI36
NG_007460.2:g.34103T>A , LRG_319:g.34103T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.374+9T>A	ENSP00000490268.2:n.374+9T>A
ENST00000585748.3:c.2+9T>A	ENSP00000477641.2:n.2+9T>A
ENST00000585851.2:c.291-1864T>A	ENSP00000467912.2:n.291-1864T>A
ENST00000326873.12:c.374+9T>A MANE Select	ENSP00000324856.6:n.374+9T>A
ENST00000652231.1:c.374+9T>A	ENSP00000498804.1:n.374+9T>A
ENST00000326873.11:c.374+9T>A	ENSP00000324856.6:n.374+9T>A
ENST00000585748.2:c.2+9T>A	ENSP00000477641.1:n.2+9T>A
ENST00000585851.1:c.291-1864T>A	ENSP00000467912.1:n.291-1864T>A
ENST00000586243.5:c.374+9T>A	ENSP00000467240.2:n.374+9T>A
ENST00000586358.5:n.197+9T>A
ENST00000589152.5:n.464+9T>A
ENST00000593219.5:c.*199+9T>A	ENSP00000466610.1:n.*199+9T>A
NM_000455.4:c.374+9T>A , LRG_319t1:c.374+9T>A	NP_000446.1:n.374+9T>A
XM_005259617.1:c.374+9T>A	XP_005259674.1:n.374+9T>A
XM_005259618.3:c.374+9T>A	XP_005259675.1:n.374+9T>A
XM_011528209.1:c.152+9T>A	XP_011526511.1:n.152+9T>A
XR_936204.1:n.999+9T>A
XM_005259617.3:c.374+9T>A	XP_005259674.1:n.374+9T>A
XM_011528209.2:c.152+9T>A	XP_011526511.1:n.152+9T>A
XR_001753738.2:n.999+9T>A
XR_001753739.1:n.999+9T>A
XR_001753740.2:n.999+9T>A
NM_000455.5:c.374+9T>A MANE Select	NP_000446.1:n.374+9T>A