Canonical Allele Identifier: CA2582597171

Gene: STK11

Linked Data

• dbSNP Id: rs2145436694
• gnomAD v4: 19-1226650-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226650C>G , CM000681.2:g.1226650C>G	GRCh38
NC_000019.9:g.1226649C>G , CM000681.1:g.1226649C>G	GRCh37
NC_000019.8:g.1177649C>G	NCBI36
NG_007460.2:g.42244C>G , LRG_319:g.42244C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2906C>G	ENSP00000490268.2:n.*2906C>G
ENST00000585748.3:c.*3C>G	ENSP00000477641.2:n.*3C>G
ENST00000585851.2:c.*3C>G	ENSP00000467912.2:n.*3C>G
ENST00000326873.12:c.*3C>G MANE Select	ENSP00000324856.6:n.*3C>G
ENST00000326873.11:c.*3C>G	ENSP00000324856.6:n.*3C>G
ENST00000585465.2:n.3038C>G
ENST00000586243.5:c.*3C>G	ENSP00000467240.2:n.*3C>G
ENST00000589152.5:n.2003C>G
NM_000455.4:c.*3C>G , LRG_319t1:c.*3C>G	NP_000446.1:n.*3C>G
XM_005259617.1:c.1300C>G	XP_005259674.1:p.Leu434Val
XM_011528209.1:c.1078C>G	XP_011526511.1:p.Leu360Val
XM_005259617.3:c.1300C>G	XP_005259674.1:p.Leu434Val
XM_011528209.2:c.1078C>G	XP_011526511.1:p.Leu360Val
XR_001753738.2:n.2111C>G
XR_001753740.2:n.2081C>G
NM_000455.5:c.*3C>G MANE Select	NP_000446.1:n.*3C>G