Canonical Allele Identifier: CA2580096039

Gene: STK11

Linked Data

• ClinVar Variation Id: 2113260
• ClinVar RCV Id: RCV003038678

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219381_1219403dup , CM000681.2:g.1219381_1219403dup	GRCh38
NC_000019.9:g.1219380_1219402dup , CM000681.1:g.1219380_1219402dup	GRCh37
NC_000019.8:g.1170380_1170402dup	NCBI36
NG_007460.2:g.34975_34997dup , LRG_319:g.34975_34997dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.432_454dup	ENSP00000490268.2:p.Gln152ArgfsTer17
ENST00000585748.3:c.60_82dup	ENSP00000477641.2:p.Gln28ArgfsTer17
ENST00000585851.2:c.291-992_291-970dup	ENSP00000467912.2:n.291-992_291-970dup
ENST00000326873.12:c.432_454dup MANE Select	ENSP00000324856.6:p.Gln152ArgfsTer17
ENST00000652231.1:c.432_454dup	ENSP00000498804.1:p.Gln152ArgfsTer17
ENST00000326873.11:c.432_454dup	ENSP00000324856.6:p.Gln152ArgfsTer17
ENST00000585851.1:c.291-992_291-970dup	ENSP00000467912.1:n.291-992_291-970dup
ENST00000586243.5:c.432_454dup	ENSP00000467240.2:p.Gln152ArgfsTer17
ENST00000586358.5:n.255_277dup
ENST00000589152.5:n.522_544dup
NM_000455.4:c.432_454dup , LRG_319t1:c.432_454dup	NP_000446.1:p.Gln152ArgfsTer17
XM_005259617.1:c.432_454dup	XP_005259674.1:p.Gln152ArgfsTer17
XM_005259618.3:c.432_454dup	XP_005259675.1:p.Gln152ArgfsTer17
XM_011528209.1:c.210_232dup	XP_011526511.1:p.Gln78ArgfsTer17
XR_936204.1:n.1057_1079dup
XM_005259617.3:c.432_454dup	XP_005259674.1:p.Gln152ArgfsTer17
XM_011528209.2:c.210_232dup	XP_011526511.1:p.Gln78ArgfsTer17
XR_001753738.2:n.1057_1079dup
XR_001753739.1:n.1057_1079dup
XR_001753740.2:n.1057_1079dup
NM_000455.5:c.432_454dup MANE Select	NP_000446.1:p.Gln152ArgfsTer17