Canonical Allele Identifier: CA2695227930

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220632_1220633del , CM000681.2:g.1220632_1220633del	GRCh38
NC_000019.9:g.1220631_1220632del , CM000681.1:g.1220631_1220632del	GRCh37
NC_000019.8:g.1171631_1171632del	NCBI36
NG_007460.2:g.36226_36227del , LRG_319:g.36226_36227del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.649_650del	ENSP00000490268.2:p.Pro217GlyfsTer?
ENST00000585748.3:c.277_278del	ENSP00000477641.2:p.Pro93GlyfsTer?
ENST00000585851.2:c.475_476del	ENSP00000467912.2:p.Pro159GlyfsTer?
ENST00000326873.12:c.649_650del MANE Select	ENSP00000324856.6:p.Pro217GlyfsTer?
ENST00000652231.1:c.649_650del	ENSP00000498804.1:p.Pro217GlyfsTer?
ENST00000326873.11:c.649_650del	ENSP00000324856.6:p.Pro217GlyfsTer?
ENST00000586243.5:c.649_650del	ENSP00000467240.2:p.Pro217GlyfsTer?
ENST00000586358.5:n.547_548del
ENST00000589152.5:n.739_740del
ENST00000591133.2:n.620_621del
NM_000455.4:c.649_650del , LRG_319t1:c.649_650del	NP_000446.1:p.Pro217GlyfsTer?
XM_005259617.1:c.649_650del	XP_005259674.1:p.Pro217GlyfsTer?
XM_005259618.3:c.649_650del	XP_005259675.1:p.Pro217GlyfsTer?
XM_011528209.1:c.427_428del	XP_011526511.1:p.Pro143GlyfsTer?
XR_936204.1:n.1274_1275del
XM_005259617.3:c.649_650del	XP_005259674.1:p.Pro217GlyfsTer?
XM_011528209.2:c.427_428del	XP_011526511.1:p.Pro143GlyfsTer?
XR_001753738.2:n.1274_1275del
XR_001753739.1:n.1274_1275del
XR_001753740.2:n.1274_1275del
NM_000455.5:c.649_650del MANE Select	NP_000446.1:p.Pro217GlyfsTer?