Canonical Allele Identifier: CA2695227940

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1223055dup , CM000681.2:g.1223055dup	GRCh38
NC_000019.9:g.1223054dup , CM000681.1:g.1223054dup	GRCh37
NC_000019.8:g.1174054dup	NCBI36
NG_007460.2:g.38649dup , LRG_319:g.38649dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.991dup	ENSP00000490268.2:p.Arg331ProfsTer29
ENST00000585748.3:c.619dup	ENSP00000477641.2:p.Arg207ProfsTer29
ENST00000585851.2:c.817dup	ENSP00000467912.2:p.Arg273ProfsTer29
ENST00000326873.12:c.991dup MANE Select	ENSP00000324856.6:p.Arg331ProfsTer29
ENST00000652231.1:c.991dup	ENSP00000498804.1:p.Arg331ProfsTer29
ENST00000326873.11:c.991dup	ENSP00000324856.6:p.Arg331ProfsTer29
ENST00000586243.5:c.991dup	ENSP00000467240.2:p.Arg331ProfsTer29
ENST00000589152.5:n.1689dup
ENST00000591133.2:n.962dup
NM_000455.4:c.991dup , LRG_319t1:c.991dup	NP_000446.1:p.Arg331ProfsTer29
XM_005259617.1:c.991dup	XP_005259674.1:p.Arg331ProfsTer29
XM_005259618.3:c.991dup	XP_005259675.1:p.Arg331ProfsTer29
XM_011528209.1:c.769dup	XP_011526511.1:p.Arg257ProfsTer29
XR_936204.1:n.1767dup
XM_005259617.3:c.991dup	XP_005259674.1:p.Arg331ProfsTer29
XM_011528209.2:c.769dup	XP_011526511.1:p.Arg257ProfsTer29
XR_001753738.2:n.1797dup
XR_001753739.1:n.1797dup
XR_001753740.2:n.1767dup
NM_000455.5:c.991dup MANE Select	NP_000446.1:p.Arg331ProfsTer29