Canonical Allele Identifier: CA2317593850

Gene: STK11

Linked Data

• dbSNP Id: rs2080825425
• gnomAD v4: 19-1226696-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226696G>A , CM000681.2:g.1226696G>A	GRCh38
NC_000019.9:g.1226695G>A , CM000681.1:g.1226695G>A	GRCh37
NC_000019.8:g.1177695G>A	NCBI36
NG_007460.2:g.42290G>A , LRG_319:g.42290G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2919+33G>A	ENSP00000490268.2:n.*2919+33G>A
ENST00000585748.3:c.*16+33G>A	ENSP00000477641.2:n.*16+33G>A
ENST00000585851.2:c.*16+33G>A	ENSP00000467912.2:n.*16+33G>A
ENST00000326873.12:c.*16+33G>A MANE Select	ENSP00000324856.6:n.*16+33G>A
ENST00000326873.11:c.*16+33G>A	ENSP00000324856.6:n.*16+33G>A
ENST00000585465.2:n.3051+33G>A
ENST00000586243.5:c.*16+33G>A	ENSP00000467240.2:n.*16+33G>A
ENST00000589152.5:n.2049G>A
NM_000455.4:c.*16+33G>A , LRG_319t1:c.*16+33G>A	NP_000446.1:n.*16+33G>A
XM_005259617.1:c.1313+33G>A	XP_005259674.1:n.1313+33G>A
XM_011528209.1:c.1091+33G>A	XP_011526511.1:n.1091+33G>A
XM_005259617.3:c.1313+33G>A	XP_005259674.1:n.1313+33G>A
XM_011528209.2:c.1091+33G>A	XP_011526511.1:n.1091+33G>A
XR_001753738.2:n.2124+33G>A
XR_001753740.2:n.2094+33G>A
NM_000455.5:c.*16+33G>A MANE Select	NP_000446.1:n.*16+33G>A