Canonical Allele Identifier: CA913190682

Gene: STK11

Linked Data

• ClinVar Variation Id: 631515
• ClinVar RCV Id: RCV000778089
• dbSNP Id: rs1568690161

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1207065dup , CM000681.2:g.1207065dup	GRCh38
NC_000019.9:g.1207064dup , CM000681.1:g.1207064dup	GRCh37
NC_000019.8:g.1158064dup	NCBI36
NG_007460.2:g.22659dup , LRG_319:g.22659dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.152dup	ENSP00000490268.2:p.Met51IlefsTer?
ENST00000585748.3:c.-82-11352dup	ENSP00000477641.2:n.-82-11352dup
ENST00000585851.2:c.152dup	ENSP00000467912.2:p.Met51IlefsTer?
ENST00000326873.12:c.152dup MANE Select	ENSP00000324856.6:p.Met51IlefsTer?
ENST00000652231.1:c.152dup	ENSP00000498804.1:p.Met51IlefsTer?
ENST00000326873.11:c.152dup	ENSP00000324856.6:p.Met51IlefsTer?
ENST00000585748.2:c.-82-11352dup	ENSP00000477641.1:n.-82-11352dup
ENST00000585851.1:c.152dup	ENSP00000467912.1:p.Met51IlefsTer?
ENST00000586243.5:c.152dup	ENSP00000467240.2:p.Met51IlefsTer?
ENST00000589152.5:n.242dup
ENST00000593219.5:c.152dup	ENSP00000466610.1:p.Met51IlefsTer?
NM_000455.4:c.152dup , LRG_319t1:c.152dup	NP_000446.1:p.Met51IlefsTer?
XM_005259617.1:c.152dup	XP_005259674.1:p.Met51IlefsTer?
XM_005259618.3:c.152dup	XP_005259675.1:p.Met51IlefsTer?
XM_011528209.1:c.-202dup	XP_011526511.1:n.-202dup
XR_936204.1:n.777dup
XM_005259617.3:c.152dup	XP_005259674.1:p.Met51IlefsTer?
XM_011528209.2:c.-202dup	XP_011526511.1:n.-202dup
XR_001753738.2:n.777dup
XR_001753739.1:n.777dup
XR_001753740.2:n.777dup
NM_000455.5:c.152dup MANE Select	NP_000446.1:p.Met51IlefsTer?