Canonical Allele Identifier: CA645604094

Gene: STK11

Linked Data

• COSMIC: COSM29466

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1221965dup , CM000681.2:g.1221965dup	GRCh38
NC_000019.9:g.1221964dup , CM000681.1:g.1221964dup	GRCh37
NC_000019.8:g.1172964dup	NCBI36
NG_007460.2:g.37559dup , LRG_319:g.37559dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.879dup	ENSP00000490268.2:p.Pro294ThrfsTer24
ENST00000585748.3:c.507dup	ENSP00000477641.2:p.Pro170ThrfsTer24
ENST00000585851.2:c.705dup	ENSP00000467912.2:p.Pro236ThrfsTer24
ENST00000326873.12:c.879dup MANE Select	ENSP00000324856.6:p.Pro294ThrfsTer24
ENST00000652231.1:c.879dup	ENSP00000498804.1:p.Pro294ThrfsTer24
ENST00000326873.11:c.879dup	ENSP00000324856.6:p.Pro294ThrfsTer24
ENST00000586243.5:c.879dup	ENSP00000467240.2:p.Pro294ThrfsTer24
ENST00000589152.5:n.1577dup
ENST00000591133.2:n.850dup
NM_000455.4:c.879dup , LRG_319t1:c.879dup	NP_000446.1:p.Pro294ThrfsTer24
XM_005259617.1:c.879dup	XP_005259674.1:p.Pro294ThrfsTer24
XM_005259618.3:c.879dup	XP_005259675.1:p.Pro294ThrfsTer24
XM_011528209.1:c.657dup	XP_011526511.1:p.Pro220ThrfsTer24
XR_936204.1:n.1655dup
XM_005259617.3:c.879dup	XP_005259674.1:p.Pro294ThrfsTer24
XM_011528209.2:c.657dup	XP_011526511.1:p.Pro220ThrfsTer24
XR_001753738.2:n.1685dup
XR_001753739.1:n.1685dup
XR_001753740.2:n.1655dup
NM_000455.5:c.879dup MANE Select	NP_000446.1:p.Pro294ThrfsTer24