Canonical Allele Identifier: CA2499225352

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1221290del , CM000681.2:g.1221290del	GRCh38
NC_000019.9:g.1221289del , CM000681.1:g.1221289del	GRCh37
NC_000019.8:g.1172289del	NCBI36
NG_007460.2:g.36884del , LRG_319:g.36884del

Transcript Alleles

HGVS	Amino-acid Change
NM_000455.5:c.812del MANE Select	NP_000446.1:p.Ser271ThrfsTer16
ENST00000326873.12:c.812del MANE Select	ENSP00000324856.6:p.Ser271ThrfsTer16
NM_000455.4:c.812del , LRG_319t1:c.812del	NP_000446.1:p.Ser271ThrfsTer16
ENST00000326873.11:c.812del	ENSP00000324856.6:p.Ser271ThrfsTer16
ENST00000585465.3:c.812del	ENSP00000490268.2:p.Ser271ThrfsTer16
ENST00000585748.3:c.440del	ENSP00000477641.2:p.Ser147ThrfsTer16
ENST00000585851.2:c.638del	ENSP00000467912.2:p.Ser213ThrfsTer16
ENST00000586243.5:c.812del	ENSP00000467240.2:p.Ser271ThrfsTer16
ENST00000586358.5:n.710del
ENST00000589152.5:n.902del
ENST00000591133.2:n.783del
ENST00000652231.1:c.812del	ENSP00000498804.1:p.Ser271ThrfsTer16
XM_005259617.1:c.812del	XP_005259674.1:p.Ser271ThrfsTer16
XM_005259617.3:c.812del	XP_005259674.1:p.Ser271ThrfsTer16
XM_005259618.3:c.812del	XP_005259675.1:p.Ser271ThrfsTer16
XM_011528209.1:c.590del	XP_011526511.1:p.Ser197ThrfsTer16
XM_011528209.2:c.590del	XP_011526511.1:p.Ser197ThrfsTer16
XR_001753738.2:n.1437del
XR_001753739.1:n.1437del
XR_001753740.2:n.1437del
XR_936204.1:n.1437del