Canonical Allele Identifier: CA2317588402

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218222_1218225delinsACCC , CM000681.2:g.1218222_1218225delinsACCC	GRCh38
NC_000019.9:g.1218221_1218224delinsACCC , CM000681.1:g.1218221_1218224delinsACCC	GRCh37
NC_000019.8:g.1169221_1169224delinsACCC	NCBI36
NG_007460.2:g.33816_33819delinsACCC , LRG_319:g.33816_33819delinsACCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.291-195_291-192delinsACCC	ENSP00000490268.2:n.291-195_291-192delinsACCC
ENST00000585748.3:c.-82-195_-82-192delinsACCC	ENSP00000477641.2:n.-82-195_-82-192delinsACCC
ENST00000585851.2:c.291-2151_291-2148delinsACCC	ENSP00000467912.2:n.291-2151_291-2148delinsACCC
ENST00000326873.12:c.291-195_291-192delinsACCC MANE Select	ENSP00000324856.6:n.291-195_291-192delinsACCC
ENST00000652231.1:c.291-195_291-192delinsACCC	ENSP00000498804.1:n.291-195_291-192delinsACCC
ENST00000326873.11:c.291-195_291-192delinsACCC	ENSP00000324856.6:n.291-195_291-192delinsACCC
ENST00000585748.2:c.-82-195_-82-192delinsACCC	ENSP00000477641.1:n.-82-195_-82-192delinsACCC
ENST00000585851.1:c.291-2151_291-2148delinsACCC	ENSP00000467912.1:n.291-2151_291-2148delinsACCC
ENST00000586243.5:c.291-195_291-192delinsACCC	ENSP00000467240.2:n.291-195_291-192delinsACCC
ENST00000586358.5:n.114-195_114-192delinsACCC
ENST00000589152.5:n.381-195_381-192delinsACCC
ENST00000593219.5:c.*116-195_*116-192delinsACCC	ENSP00000466610.1:n.*116-195_*116-192delinsACCC
NM_000455.4:c.291-195_291-192delinsACCC , LRG_319t1:c.291-195_291-192delinsACCC	NP_000446.1:n.291-195_291-192delinsACCC
XM_005259617.1:c.291-195_291-192delinsACCC	XP_005259674.1:n.291-195_291-192delinsACCC
XM_005259618.3:c.291-195_291-192delinsACCC	XP_005259675.1:n.291-195_291-192delinsACCC
XM_011528209.1:c.69-195_69-192delinsACCC	XP_011526511.1:n.69-195_69-192delinsACCC
XR_936204.1:n.916-195_916-192delinsACCC
XM_005259617.3:c.291-195_291-192delinsACCC	XP_005259674.1:n.291-195_291-192delinsACCC
XM_011528209.2:c.69-195_69-192delinsACCC	XP_011526511.1:n.69-195_69-192delinsACCC
XR_001753738.2:n.916-195_916-192delinsACCC
XR_001753739.1:n.916-195_916-192delinsACCC
XR_001753740.2:n.916-195_916-192delinsACCC
NM_000455.5:c.291-195_291-192delinsACCC MANE Select	NP_000446.1:n.291-195_291-192delinsACCC