Canonical Allele Identifier: CA1139770835

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219409del , CM000681.2:g.1219409del	GRCh38
NC_000019.9:g.1219408del , CM000681.1:g.1219408del	GRCh37
NC_000019.8:g.1170408del	NCBI36
NG_007460.2:g.35003del , LRG_319:g.35003del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.460del	ENSP00000490268.2:p.His154ThrfsTer7
ENST00000585748.3:c.88del	ENSP00000477641.2:p.His30ThrfsTer7
ENST00000585851.2:c.291-964del	ENSP00000467912.2:n.291-964del
ENST00000326873.12:c.460del MANE Select	ENSP00000324856.6:p.His154ThrfsTer7
ENST00000652231.1:c.460del	ENSP00000498804.1:p.His154ThrfsTer7
ENST00000326873.11:c.460del	ENSP00000324856.6:p.His154ThrfsTer7
ENST00000585851.1:c.291-964del	ENSP00000467912.1:n.291-964del
ENST00000586243.5:c.460del	ENSP00000467240.2:p.His154ThrfsTer7
ENST00000586358.5:n.283del
ENST00000589152.5:n.550del
NM_000455.4:c.460del , LRG_319t1:c.460del	NP_000446.1:p.His154ThrfsTer7
XM_005259617.1:c.460del	XP_005259674.1:p.His154ThrfsTer7
XM_005259618.3:c.460del	XP_005259675.1:p.His154ThrfsTer7
XM_011528209.1:c.238del	XP_011526511.1:p.His80ThrfsTer7
XR_936204.1:n.1085del
XM_005259617.3:c.460del	XP_005259674.1:p.His154ThrfsTer7
XM_011528209.2:c.238del	XP_011526511.1:p.His80ThrfsTer7
XR_001753738.2:n.1085del
XR_001753739.1:n.1085del
XR_001753740.2:n.1085del
NM_000455.5:c.460del MANE Select	NP_000446.1:p.His154ThrfsTer7