Canonical Allele Identifier: CA402948885

Gene: STK11

Linked Data

• dbSNP Id: rs2145424257
• gnomAD v4: 19-1220407-C-A
• MyVariant Identifiers: chr19:g.1220406C>A (hg19) ; chr19:g.1220407C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220407C>A , CM000681.2:g.1220407C>A	GRCh38
NC_000019.9:g.1220406C>A , CM000681.1:g.1220406C>A	GRCh37
NC_000019.8:g.1171406C>A	NCBI36
NG_007460.2:g.36001C>A , LRG_319:g.36001C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.499C>A	ENSP00000490268.2:p.Leu167Met
ENST00000585748.3:c.127C>A	ENSP00000477641.2:p.Leu43Met
ENST00000585851.2:c.325C>A	ENSP00000467912.2:p.Leu109Met
ENST00000326873.12:c.499C>A MANE Select	ENSP00000324856.6:p.Leu167Met
ENST00000652231.1:c.499C>A	ENSP00000498804.1:p.Leu167Met
ENST00000326873.11:c.499C>A	ENSP00000324856.6:p.Leu167Met
ENST00000585851.1:c.325C>A	ENSP00000467912.1:p.Leu109Met
ENST00000586243.5:c.499C>A	ENSP00000467240.2:p.Leu167Met
ENST00000586358.5:n.322C>A
ENST00000589152.5:n.589C>A
ENST00000591133.2:n.395C>A
NM_000455.4:c.499C>A , LRG_319t1:c.499C>A	NP_000446.1:p.Leu167Met
XM_005259617.1:c.499C>A	XP_005259674.1:p.Leu167Met
XM_005259618.3:c.499C>A	XP_005259675.1:p.Leu167Met
XM_011528209.1:c.277C>A	XP_011526511.1:p.Leu93Met
XR_936204.1:n.1124C>A
XM_005259617.3:c.499C>A	XP_005259674.1:p.Leu167Met
XM_011528209.2:c.277C>A	XP_011526511.1:p.Leu93Met
XR_001753738.2:n.1124C>A
XR_001753739.1:n.1124C>A
XR_001753740.2:n.1124C>A
NM_000455.5:c.499C>A MANE Select	NP_000446.1:p.Leu167Met