Canonical Allele Identifier: CA402943072

Gene: STK11

Linked Data

• ClinVar Variation Id: 2002561
• ClinVar RCV Id: RCV002833003
• dbSNP Id: rs760588289
• gnomAD v3: 19-1206935-C-A
• gnomAD v4: 19-1206935-C-A
• MyVariant Identifiers: chr19:g.1206934C>A (hg19) ; chr19:g.1206935C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1206935C>A , CM000681.2:g.1206935C>A	GRCh38
NC_000019.9:g.1206934C>A , CM000681.1:g.1206934C>A	GRCh37
NC_000019.8:g.1157934C>A	NCBI36
NG_007460.2:g.22529C>A , LRG_319:g.22529C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.22C>A	ENSP00000490268.2:p.Gln8Lys
ENST00000585748.3:c.-82-11482C>A	ENSP00000477641.2:n.-82-11482C>A
ENST00000585851.2:c.22C>A	ENSP00000467912.2:p.Gln8Lys
ENST00000326873.12:c.22C>A MANE Select	ENSP00000324856.6:p.Gln8Lys
ENST00000652231.1:c.22C>A	ENSP00000498804.1:p.Gln8Lys
ENST00000326873.11:c.22C>A	ENSP00000324856.6:p.Gln8Lys
ENST00000585748.2:c.-82-11482C>A	ENSP00000477641.1:n.-82-11482C>A
ENST00000585851.1:c.22C>A	ENSP00000467912.1:p.Gln8Lys
ENST00000586243.5:c.22C>A	ENSP00000467240.2:p.Gln8Lys
ENST00000589152.5:n.112C>A
ENST00000593219.5:c.22C>A	ENSP00000466610.1:p.Gln8Lys
NM_000455.4:c.22C>A , LRG_319t1:c.22C>A	NP_000446.1:p.Gln8Lys
XM_005259617.1:c.22C>A	XP_005259674.1:p.Gln8Lys
XM_005259618.3:c.22C>A	XP_005259675.1:p.Gln8Lys
XM_011528209.1:c.-332C>A	XP_011526511.1:n.-332C>A
XR_936204.1:n.647C>A
XM_005259617.3:c.22C>A	XP_005259674.1:p.Gln8Lys
XM_011528209.2:c.-332C>A	XP_011526511.1:n.-332C>A
XR_001753738.2:n.647C>A
XR_001753739.1:n.647C>A
XR_001753740.2:n.647C>A
NM_000455.5:c.22C>A MANE Select	NP_000446.1:p.Gln8Lys