Canonical Allele Identifier: CA304024093

Gene: STK11

Linked Data

• dbSNP Id: rs547292293
• gnomAD v2: 19-1218247-C-A
• gnomAD v3: 19-1218248-C-A
• gnomAD v4: 19-1218248-C-A
• MyVariant Identifiers: chr19:g.1218247C>A (hg19) ; chr19:g.1218248C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218248C>A , CM000681.2:g.1218248C>A	GRCh38
NC_000019.9:g.1218247C>A , CM000681.1:g.1218247C>A	GRCh37
NC_000019.8:g.1169247C>A	NCBI36
NG_007460.2:g.33842C>A , LRG_319:g.33842C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.291-169C>A	ENSP00000490268.2:n.291-169C>A
ENST00000585748.3:c.-82-169C>A	ENSP00000477641.2:n.-82-169C>A
ENST00000585851.2:c.291-2125C>A	ENSP00000467912.2:n.291-2125C>A
ENST00000326873.12:c.291-169C>A MANE Select	ENSP00000324856.6:n.291-169C>A
ENST00000652231.1:c.291-169C>A	ENSP00000498804.1:n.291-169C>A
ENST00000326873.11:c.291-169C>A	ENSP00000324856.6:n.291-169C>A
ENST00000585748.2:c.-82-169C>A	ENSP00000477641.1:n.-82-169C>A
ENST00000585851.1:c.291-2125C>A	ENSP00000467912.1:n.291-2125C>A
ENST00000586243.5:c.291-169C>A	ENSP00000467240.2:n.291-169C>A
ENST00000586358.5:n.114-169C>A
ENST00000589152.5:n.381-169C>A
ENST00000593219.5:c.*116-169C>A	ENSP00000466610.1:n.*116-169C>A
NM_000455.4:c.291-169C>A , LRG_319t1:c.291-169C>A	NP_000446.1:n.291-169C>A
XM_005259617.1:c.291-169C>A	XP_005259674.1:n.291-169C>A
XM_005259618.3:c.291-169C>A	XP_005259675.1:n.291-169C>A
XM_011528209.1:c.69-169C>A	XP_011526511.1:n.69-169C>A
XR_936204.1:n.916-169C>A
XM_005259617.3:c.291-169C>A	XP_005259674.1:n.291-169C>A
XM_011528209.2:c.69-169C>A	XP_011526511.1:n.69-169C>A
XR_001753738.2:n.916-169C>A
XR_001753739.1:n.916-169C>A
XR_001753740.2:n.916-169C>A
NM_000455.5:c.291-169C>A MANE Select	NP_000446.1:n.291-169C>A