Canonical Allele Identifier: CA2526520121

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218307_1218311del , CM000681.2:g.1218307_1218311del	GRCh38
NC_000019.9:g.1218306_1218310del , CM000681.1:g.1218306_1218310del	GRCh37
NC_000019.8:g.1169306_1169310del	NCBI36
NG_007460.2:g.33901_33905del , LRG_319:g.33901_33905del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.291-110_291-106del	ENSP00000490268.2:n.291-110_291-106del
ENST00000585748.3:c.-82-110_-82-106del	ENSP00000477641.2:n.-82-110_-82-106del
ENST00000585851.2:c.291-2066_291-2062del	ENSP00000467912.2:n.291-2066_291-2062del
ENST00000326873.12:c.291-110_291-106del MANE Select	ENSP00000324856.6:n.291-110_291-106del
ENST00000652231.1:c.291-110_291-106del	ENSP00000498804.1:n.291-110_291-106del
ENST00000326873.11:c.291-110_291-106del	ENSP00000324856.6:n.291-110_291-106del
ENST00000585748.2:c.-82-110_-82-106del	ENSP00000477641.1:n.-82-110_-82-106del
ENST00000585851.1:c.291-2066_291-2062del	ENSP00000467912.1:n.291-2066_291-2062del
ENST00000586243.5:c.291-110_291-106del	ENSP00000467240.2:n.291-110_291-106del
ENST00000586358.5:n.114-110_114-106del
ENST00000589152.5:n.381-110_381-106del
ENST00000593219.5:c.*116-110_*116-106del	ENSP00000466610.1:n.*116-110_*116-106del
NM_000455.4:c.291-110_291-106del , LRG_319t1:c.291-110_291-106del	NP_000446.1:n.291-110_291-106del
XM_005259617.1:c.291-110_291-106del	XP_005259674.1:n.291-110_291-106del
XM_005259618.3:c.291-110_291-106del	XP_005259675.1:n.291-110_291-106del
XM_011528209.1:c.69-110_69-106del	XP_011526511.1:n.69-110_69-106del
XR_936204.1:n.916-110_916-106del
XM_005259617.3:c.291-110_291-106del	XP_005259674.1:n.291-110_291-106del
XM_011528209.2:c.69-110_69-106del	XP_011526511.1:n.69-110_69-106del
XR_001753738.2:n.916-110_916-106del
XR_001753739.1:n.916-110_916-106del
XR_001753740.2:n.916-110_916-106del
NM_000455.5:c.291-110_291-106del MANE Select	NP_000446.1:n.291-110_291-106del