Canonical Allele Identifier: CA2739291134

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220615_1220631del , CM000681.2:g.1220615_1220631del	GRCh38
NC_000019.9:g.1220614_1220630del , CM000681.1:g.1220614_1220630del	GRCh37
NC_000019.8:g.1171614_1171630del	NCBI36
NG_007460.2:g.36209_36225del , LRG_319:g.36209_36225del

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.632_648del	ENSP00000490268.2:p.Arg211ProfsTer?
ENST00000585748.3:c.260_276del	ENSP00000477641.2:p.Arg87ProfsTer?
ENST00000585851.2:c.458_474del	ENSP00000467912.2:p.Arg153ProfsTer?
ENST00000326873.12:c.632_648del MANE Select	ENSP00000324856.6:p.Arg211ProfsTer?
ENST00000652231.1:c.632_648del	ENSP00000498804.1:p.Arg211ProfsTer?
ENST00000326873.11:c.632_648del	ENSP00000324856.6:p.Arg211ProfsTer?
ENST00000586243.5:c.632_648del	ENSP00000467240.2:p.Arg211ProfsTer?
ENST00000586358.5:n.530_546del
ENST00000589152.5:n.722_738del
ENST00000591133.2:n.603_619del
NM_000455.4:c.632_648del , LRG_319t1:c.632_648del	NP_000446.1:p.Arg211ProfsTer?
XM_005259617.1:c.632_648del	XP_005259674.1:p.Arg211ProfsTer?
XM_005259618.3:c.632_648del	XP_005259675.1:p.Arg211ProfsTer?
XM_011528209.1:c.410_426del	XP_011526511.1:p.Arg137ProfsTer?
XR_936204.1:n.1257_1273del
XM_005259617.3:c.632_648del	XP_005259674.1:p.Arg211ProfsTer?
XM_011528209.2:c.410_426del	XP_011526511.1:p.Arg137ProfsTer?
XR_001753738.2:n.1257_1273del
XR_001753739.1:n.1257_1273del
XR_001753740.2:n.1257_1273del
NM_000455.5:c.632_648del MANE Select	NP_000446.1:p.Arg211ProfsTer?