Canonical Allele Identifier: CA2582597179

Gene: STK11

Linked Data

• dbSNP Id: rs2145435704
• gnomAD v4: 19-1226431-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226431C>A , CM000681.2:g.1226431C>A	GRCh38
NC_000019.9:g.1226430C>A , CM000681.1:g.1226430C>A	GRCh37
NC_000019.8:g.1177430C>A	NCBI36
NG_007460.2:g.42025C>A , LRG_319:g.42025C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2687C>A	ENSP00000490268.2:n.*2687C>A
ENST00000585748.3:c.737-23C>A	ENSP00000477641.2:n.737-23C>A
ENST00000585851.2:c.935-23C>A	ENSP00000467912.2:n.935-23C>A
ENST00000326873.12:c.1109-23C>A MANE Select	ENSP00000324856.6:n.1109-23C>A
ENST00000326873.11:c.1109-23C>A	ENSP00000324856.6:n.1109-23C>A
ENST00000585465.2:n.2819C>A
ENST00000586243.5:c.1109-23C>A	ENSP00000467240.2:n.1109-23C>A
ENST00000589152.5:n.1807-23C>A
NM_000455.4:c.1109-23C>A , LRG_319t1:c.1109-23C>A	NP_000446.1:n.1109-23C>A
XM_005259617.1:c.1109-28C>A	XP_005259674.1:n.1109-28C>A
XM_011528209.1:c.887-28C>A	XP_011526511.1:n.887-28C>A
XM_005259617.3:c.1109-28C>A	XP_005259674.1:n.1109-28C>A
XM_011528209.2:c.887-28C>A	XP_011526511.1:n.887-28C>A
XR_001753738.2:n.1915-23C>A
XR_001753740.2:n.1885-23C>A
NM_000455.5:c.1109-23C>A MANE Select	NP_000446.1:n.1109-23C>A