Canonical Allele Identifier: CA2525773532

Gene: STK11

Linked Data

• ClinVar Variation Id: 1638890
• ClinVar RCV Id: RCV002126524
• dbSNP Id: rs2080777425

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220730C>G , CM000681.2:g.1220730C>G	GRCh38
NC_000019.9:g.1220729C>G , CM000681.1:g.1220729C>G	GRCh37
NC_000019.8:g.1171729C>G	NCBI36
NG_007460.2:g.36324C>G , LRG_319:g.36324C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.734+13C>G	ENSP00000490268.2:n.734+13C>G
ENST00000585748.3:c.362+13C>G	ENSP00000477641.2:n.362+13C>G
ENST00000585851.2:c.560+13C>G	ENSP00000467912.2:n.560+13C>G
ENST00000326873.12:c.734+13C>G MANE Select	ENSP00000324856.6:n.734+13C>G
ENST00000652231.1:c.734+13C>G	ENSP00000498804.1:n.734+13C>G
ENST00000326873.11:c.734+13C>G	ENSP00000324856.6:n.734+13C>G
ENST00000586243.5:c.734+13C>G	ENSP00000467240.2:n.734+13C>G
ENST00000586358.5:n.632+13C>G
ENST00000589152.5:n.824+13C>G
ENST00000591133.2:n.705+13C>G
NM_000455.4:c.734+13C>G , LRG_319t1:c.734+13C>G	NP_000446.1:n.734+13C>G
XM_005259617.1:c.734+13C>G	XP_005259674.1:n.734+13C>G
XM_005259618.3:c.734+13C>G	XP_005259675.1:n.734+13C>G
XM_011528209.1:c.512+13C>G	XP_011526511.1:n.512+13C>G
XR_936204.1:n.1359+13C>G
XM_005259617.3:c.734+13C>G	XP_005259674.1:n.734+13C>G
XM_011528209.2:c.512+13C>G	XP_011526511.1:n.512+13C>G
XR_001753738.2:n.1359+13C>G
XR_001753739.1:n.1359+13C>G
XR_001753740.2:n.1359+13C>G
NM_000455.5:c.734+13C>G MANE Select	NP_000446.1:n.734+13C>G