Canonical Allele Identifier: CA504707776

Gene: STK11

Linked Data

• ClinVar Variation Id: 527840
• ClinVar RCV Id: RCV000632842 ; RCV002385992
• dbSNP Id: rs1195673013
• gnomAD v2: 19-1223089-G-A
• gnomAD v4: 19-1223090-G-A
• MyVariant Identifiers: chr19:g.1223089G>A (hg19) ; chr19:g.1223090G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1223090G>A , CM000681.2:g.1223090G>A	GRCh38
NC_000019.9:g.1223089G>A , CM000681.1:g.1223089G>A	GRCh37
NC_000019.8:g.1174089G>A	NCBI36
NG_007460.2:g.38684G>A , LRG_319:g.38684G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.1026G>A	ENSP00000490268.2:p.Glu342=
ENST00000585748.3:c.654G>A	ENSP00000477641.2:p.Glu218=
ENST00000585851.2:c.852G>A	ENSP00000467912.2:p.Glu284=
ENST00000326873.12:c.1026G>A MANE Select	ENSP00000324856.6:p.Glu342=
ENST00000652231.1:c.1026G>A	ENSP00000498804.1:p.Glu342=
ENST00000326873.11:c.1026G>A	ENSP00000324856.6:p.Glu342=
ENST00000586243.5:c.1026G>A	ENSP00000467240.2:p.Glu342=
ENST00000589152.5:n.1724G>A
ENST00000591133.2:n.997G>A
NM_000455.4:c.1026G>A , LRG_319t1:c.1026G>A	NP_000446.1:p.Glu342=
XM_005259617.1:c.1026G>A	XP_005259674.1:p.Glu342=
XM_005259618.3:c.1026G>A	XP_005259675.1:p.Glu342=
XM_011528209.1:c.804G>A	XP_011526511.1:p.Glu268=
XR_936204.1:n.1802G>A
XM_005259617.3:c.1026G>A	XP_005259674.1:p.Glu342=
XM_011528209.2:c.804G>A	XP_011526511.1:p.Glu268=
XR_001753738.2:n.1832G>A
XR_001753739.1:n.1832G>A
XR_001753740.2:n.1802G>A
NM_000455.5:c.1026G>A MANE Select	NP_000446.1:p.Glu342=