Canonical Allele Identifier: CA915951587

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1221250del , CM000681.2:g.1221250del	GRCh38
NC_000019.9:g.1221249del , CM000681.1:g.1221249del	GRCh37
NC_000019.8:g.1172249del	NCBI36
NG_007460.2:g.36844del , LRG_319:g.36844del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.772del	ENSP00000490268.2:p.Asp258ThrfsTer29
ENST00000585748.3:c.400del	ENSP00000477641.2:p.Asp134ThrfsTer29
ENST00000585851.2:c.598del	ENSP00000467912.2:p.Asp200ThrfsTer29
ENST00000326873.12:c.772del MANE Select	ENSP00000324856.6:p.Asp258ThrfsTer29
ENST00000652231.1:c.772del	ENSP00000498804.1:p.Asp258ThrfsTer29
ENST00000326873.11:c.772del	ENSP00000324856.6:p.Asp258ThrfsTer29
ENST00000586243.5:c.772del	ENSP00000467240.2:p.Asp258ThrfsTer29
ENST00000586358.5:n.670del
ENST00000589152.5:n.862del
ENST00000591133.2:n.743del
NM_000455.4:c.772del , LRG_319t1:c.772del	NP_000446.1:p.Asp258ThrfsTer29
XM_005259617.1:c.772del	XP_005259674.1:p.Asp258ThrfsTer29
XM_005259618.3:c.772del	XP_005259675.1:p.Asp258ThrfsTer29
XM_011528209.1:c.550del	XP_011526511.1:p.Asp184ThrfsTer29
XR_936204.1:n.1397del
XM_005259617.3:c.772del	XP_005259674.1:p.Asp258ThrfsTer29
XM_011528209.2:c.550del	XP_011526511.1:p.Asp184ThrfsTer29
XR_001753738.2:n.1397del
XR_001753739.1:n.1397del
XR_001753740.2:n.1397del
NM_000455.5:c.772del MANE Select	NP_000446.1:p.Asp258ThrfsTer29