Canonical Allele Identifier: CA2966064279

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218384dup , CM000681.2:g.1218384dup	GRCh38
NC_000019.9:g.1218383dup , CM000681.1:g.1218383dup	GRCh37
NC_000019.8:g.1169383dup	NCBI36
NG_007460.2:g.33978dup , LRG_319:g.33978dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.291-33dup	ENSP00000490268.2:n.291-33dup
ENST00000585748.3:c.-82-33dup	ENSP00000477641.2:n.-82-33dup
ENST00000585851.2:c.291-1989dup	ENSP00000467912.2:n.291-1989dup
ENST00000326873.12:c.291-33dup MANE Select	ENSP00000324856.6:n.291-33dup
ENST00000652231.1:c.291-33dup	ENSP00000498804.1:n.291-33dup
ENST00000326873.11:c.291-33dup	ENSP00000324856.6:n.291-33dup
ENST00000585748.2:c.-82-33dup	ENSP00000477641.1:n.-82-33dup
ENST00000585851.1:c.291-1989dup	ENSP00000467912.1:n.291-1989dup
ENST00000586243.5:c.291-33dup	ENSP00000467240.2:n.291-33dup
ENST00000586358.5:n.114-33dup
ENST00000589152.5:n.381-33dup
ENST00000593219.5:c.*116-33dup	ENSP00000466610.1:n.*116-33dup
NM_000455.4:c.291-33dup , LRG_319t1:c.291-33dup	NP_000446.1:n.291-33dup
XM_005259617.1:c.291-33dup	XP_005259674.1:n.291-33dup
XM_005259618.3:c.291-33dup	XP_005259675.1:n.291-33dup
XM_011528209.1:c.69-33dup	XP_011526511.1:n.69-33dup
XR_936204.1:n.916-33dup
XM_005259617.3:c.291-33dup	XP_005259674.1:n.291-33dup
XM_011528209.2:c.69-33dup	XP_011526511.1:n.69-33dup
XR_001753738.2:n.916-33dup
XR_001753739.1:n.916-33dup
XR_001753740.2:n.916-33dup
NM_000455.5:c.291-33dup MANE Select	NP_000446.1:n.291-33dup