Canonical Allele Identifier: CA2695227875

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219373_1219377dup , CM000681.2:g.1219373_1219377dup	GRCh38
NC_000019.9:g.1219372_1219376dup , CM000681.1:g.1219372_1219376dup	GRCh37
NC_000019.8:g.1170372_1170376dup	NCBI36
NG_007460.2:g.34967_34971dup , LRG_319:g.34967_34971dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.424_428dup	ENSP00000490268.2:p.Pro144AlafsTer19
ENST00000585748.3:c.52_56dup	ENSP00000477641.2:p.Pro20AlafsTer19
ENST00000585851.2:c.291-1000_291-996dup	ENSP00000467912.2:n.291-1000_291-996dup
ENST00000326873.12:c.424_428dup MANE Select	ENSP00000324856.6:p.Pro144AlafsTer19
ENST00000652231.1:c.424_428dup	ENSP00000498804.1:p.Pro144AlafsTer19
ENST00000326873.11:c.424_428dup	ENSP00000324856.6:p.Pro144AlafsTer19
ENST00000585748.2:c.52_56dup	ENSP00000477641.1:p.Pro20AlafsTer?
ENST00000585851.1:c.291-1000_291-996dup	ENSP00000467912.1:n.291-1000_291-996dup
ENST00000586243.5:c.424_428dup	ENSP00000467240.2:p.Pro144AlafsTer19
ENST00000586358.5:n.247_251dup
ENST00000589152.5:n.514_518dup
NM_000455.4:c.424_428dup , LRG_319t1:c.424_428dup	NP_000446.1:p.Pro144AlafsTer19
XM_005259617.1:c.424_428dup	XP_005259674.1:p.Pro144AlafsTer19
XM_005259618.3:c.424_428dup	XP_005259675.1:p.Pro144AlafsTer19
XM_011528209.1:c.202_206dup	XP_011526511.1:p.Pro70AlafsTer19
XR_936204.1:n.1049_1053dup
XM_005259617.3:c.424_428dup	XP_005259674.1:p.Pro144AlafsTer19
XM_011528209.2:c.202_206dup	XP_011526511.1:p.Pro70AlafsTer19
XR_001753738.2:n.1049_1053dup
XR_001753739.1:n.1049_1053dup
XR_001753740.2:n.1049_1053dup
NM_000455.5:c.424_428dup MANE Select	NP_000446.1:p.Pro144AlafsTer19