Canonical Allele Identifier: CA2582591745

Gene: STK11

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218290_1218291del , CM000681.2:g.1218290_1218291del	GRCh38
NC_000019.9:g.1218289_1218290del , CM000681.1:g.1218289_1218290del	GRCh37
NC_000019.8:g.1169289_1169290del	NCBI36
NG_007460.2:g.33884_33885del , LRG_319:g.33884_33885del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.291-127_291-126del	ENSP00000490268.2:n.291-127_291-126del
ENST00000585748.3:c.-82-127_-82-126del	ENSP00000477641.2:n.-82-127_-82-126del
ENST00000585851.2:c.291-2083_291-2082del	ENSP00000467912.2:n.291-2083_291-2082del
ENST00000326873.12:c.291-127_291-126del MANE Select	ENSP00000324856.6:n.291-127_291-126del
ENST00000652231.1:c.291-127_291-126del	ENSP00000498804.1:n.291-127_291-126del
ENST00000326873.11:c.291-127_291-126del	ENSP00000324856.6:n.291-127_291-126del
ENST00000585748.2:c.-82-127_-82-126del	ENSP00000477641.1:n.-82-127_-82-126del
ENST00000585851.1:c.291-2083_291-2082del	ENSP00000467912.1:n.291-2083_291-2082del
ENST00000586243.5:c.291-127_291-126del	ENSP00000467240.2:n.291-127_291-126del
ENST00000586358.5:n.114-127_114-126del
ENST00000589152.5:n.381-127_381-126del
ENST00000593219.5:c.*116-127_*116-126del	ENSP00000466610.1:n.*116-127_*116-126del
NM_000455.4:c.291-127_291-126del , LRG_319t1:c.291-127_291-126del	NP_000446.1:n.291-127_291-126del
XM_005259617.1:c.291-127_291-126del	XP_005259674.1:n.291-127_291-126del
XM_005259618.3:c.291-127_291-126del	XP_005259675.1:n.291-127_291-126del
XM_011528209.1:c.69-127_69-126del	XP_011526511.1:n.69-127_69-126del
XR_936204.1:n.916-127_916-126del
XM_005259617.3:c.291-127_291-126del	XP_005259674.1:n.291-127_291-126del
XM_011528209.2:c.69-127_69-126del	XP_011526511.1:n.69-127_69-126del
XR_001753738.2:n.916-127_916-126del
XR_001753739.1:n.916-127_916-126del
XR_001753740.2:n.916-127_916-126del
NM_000455.5:c.291-127_291-126del MANE Select	NP_000446.1:n.291-127_291-126del