Canonical Allele Identifier: CA504708418

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226494C>A , CM000681.2:g.1226494C>A	GRCh38
NC_000019.9:g.1226493C>A , CM000681.1:g.1226493C>A	GRCh37
NC_000019.8:g.1177493C>A	NCBI36
NG_007460.2:g.42088C>A , LRG_319:g.42088C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000455.5:c.1149C>A MANE Select	NP_000446.1:p.Arg383=
ENST00000326873.12:c.1149C>A MANE Select	ENSP00000324856.6:p.Arg383=
NM_000455.4:c.1149C>A , LRG_319t1:c.1149C>A	NP_000446.1:p.Arg383=
ENST00000326873.11:c.1149C>A	ENSP00000324856.6:p.Arg383=
ENST00000585465.2:n.2882C>A
ENST00000585465.3:c.*2750C>A	ENSP00000490268.2:n.*2750C>A
ENST00000585748.3:c.777C>A	ENSP00000477641.2:p.Arg259=
ENST00000585851.2:c.975C>A	ENSP00000467912.2:p.Arg325=
ENST00000586243.5:c.1149C>A	ENSP00000467240.2:p.Arg383=
ENST00000589152.5:n.1847C>A
XM_005259617.1:c.1144C>A	XP_005259674.1:p.Pro382Thr
XM_005259617.3:c.1144C>A	XP_005259674.1:p.Pro382Thr
XM_011528209.1:c.922C>A	XP_011526511.1:p.Pro308Thr
XM_011528209.2:c.922C>A	XP_011526511.1:p.Pro308Thr
XR_001753738.2:n.1955C>A
XR_001753740.2:n.1925C>A