Canonical Allele Identifier: CA10642309

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1227989C>A , CM000681.2:g.1227989C>A	GRCh38
NC_000019.9:g.1227988C>A , CM000681.1:g.1227988C>A	GRCh37
NC_000019.8:g.1178988C>A	NCBI36
NG_007460.2:g.43583C>A , LRG_319:g.43583C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000455.5:c.*413C>A MANE Select	NP_000446.1:n.*413C>A
ENST00000326873.12:c.*413C>A MANE Select	ENSP00000324856.6:n.*413C>A
NM_000455.4:c.*413C>A , LRG_319t1:c.*413C>A	NP_000446.1:n.*413C>A
ENST00000326873.11:c.*413C>A	ENSP00000324856.6:n.*413C>A
ENST00000585465.2:n.3448C>A
ENST00000585465.3:c.*3316C>A	ENSP00000490268.2:n.*3316C>A
ENST00000585748.3:c.*413C>A	ENSP00000477641.2:n.*413C>A
ENST00000585851.2:c.*413C>A	ENSP00000467912.2:n.*413C>A
ENST00000586243.5:c.*413C>A	ENSP00000467240.2:n.*413C>A
ENST00000589152.5:n.3342C>A
XM_005259617.1:c.1710C>A	XP_005259674.1:p.Cys570Ter
XM_005259617.3:c.1710C>A	XP_005259674.1:p.Cys570Ter
XM_011528209.1:c.1488C>A	XP_011526511.1:p.Cys496Ter
XM_011528209.2:c.1488C>A	XP_011526511.1:p.Cys496Ter
XR_001753738.2:n.2521C>A
XR_001753740.2:n.2491C>A