Canonical Allele Identifier: CA992502908

Gene: STK11

Linked Data

• dbSNP Id: rs911055521
• gnomAD v3: 19-1206796-C-A
• gnomAD v4: 19-1206796-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1206796C>A , CM000681.2:g.1206796C>A	GRCh38
NC_000019.9:g.1206795C>A , CM000681.1:g.1206795C>A	GRCh37
NC_000019.8:g.1157795C>A	NCBI36
NG_007460.2:g.22390C>A , LRG_319:g.22390C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.-118C>A	ENSP00000490268.2:n.-118C>A
ENST00000585748.3:c.-82-11621C>A	ENSP00000477641.2:n.-82-11621C>A
ENST00000326873.12:c.-118C>A MANE Select	ENSP00000324856.6:n.-118C>A
ENST00000652231.1:c.-118C>A	ENSP00000498804.1:n.-118C>A
ENST00000326873.11:c.-118C>A	ENSP00000324856.6:n.-118C>A
ENST00000585748.2:c.-82-11621C>A	ENSP00000477641.1:n.-82-11621C>A
ENST00000586243.5:c.-118C>A	ENSP00000467240.2:n.-118C>A
NM_000455.4:c.-118C>A , LRG_319t1:c.-118C>A	NP_000446.1:n.-118C>A
XM_005259617.1:c.-118C>A	XP_005259674.1:n.-118C>A
XM_005259618.3:c.-118C>A	XP_005259675.1:n.-118C>A
XM_011528209.1:c.-471C>A	XP_011526511.1:n.-471C>A
XR_936204.1:n.508C>A
XM_005259617.3:c.-118C>A	XP_005259674.1:n.-118C>A
XM_011528209.2:c.-471C>A	XP_011526511.1:n.-471C>A
XR_001753738.2:n.508C>A
XR_001753739.1:n.508C>A
XR_001753740.2:n.508C>A
NM_000455.5:c.-118C>A MANE Select	NP_000446.1:n.-118C>A