Canonical Allele Identifier: CA645604087

Gene: STK11

Linked Data

• COSMIC: COSM27281

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220632_1220633insG , CM000681.2:g.1220632_1220633insG	GRCh38
NC_000019.9:g.1220631_1220632insG , CM000681.1:g.1220631_1220632insG	GRCh37
NC_000019.8:g.1171631_1171632insG	NCBI36
NG_007460.2:g.36226_36227insG , LRG_319:g.36226_36227insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.649_650insG	ENSP00000490268.2:p.Pro217ArgfsTer?
ENST00000585748.3:c.277_278insG	ENSP00000477641.2:p.Pro93ArgfsTer?
ENST00000585851.2:c.475_476insG	ENSP00000467912.2:p.Pro159ArgfsTer?
ENST00000326873.12:c.649_650insG MANE Select	ENSP00000324856.6:p.Pro217ArgfsTer?
ENST00000652231.1:c.649_650insG	ENSP00000498804.1:p.Pro217ArgfsTer?
ENST00000326873.11:c.649_650insG	ENSP00000324856.6:p.Pro217ArgfsTer?
ENST00000586243.5:c.649_650insG	ENSP00000467240.2:p.Pro217ArgfsTer?
ENST00000586358.5:n.547_548insG
ENST00000589152.5:n.739_740insG
ENST00000591133.2:n.620_621insG
NM_000455.4:c.649_650insG , LRG_319t1:c.649_650insG	NP_000446.1:p.Pro217ArgfsTer?
XM_005259617.1:c.649_650insG	XP_005259674.1:p.Pro217ArgfsTer?
XM_005259618.3:c.649_650insG	XP_005259675.1:p.Pro217ArgfsTer?
XM_011528209.1:c.427_428insG	XP_011526511.1:p.Pro143ArgfsTer?
XR_936204.1:n.1274_1275insG
XM_005259617.3:c.649_650insG	XP_005259674.1:p.Pro217ArgfsTer?
XM_011528209.2:c.427_428insG	XP_011526511.1:p.Pro143ArgfsTer?
XR_001753738.2:n.1274_1275insG
XR_001753739.1:n.1274_1275insG
XR_001753740.2:n.1274_1275insG
NM_000455.5:c.649_650insG MANE Select	NP_000446.1:p.Pro217ArgfsTer?