Canonical Allele Identifier: CA658655480

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1223026_1223027del , CM000681.2:g.1223026_1223027del	GRCh38
NC_000019.9:g.1223025_1223026del , CM000681.1:g.1223025_1223026del	GRCh37
NC_000019.8:g.1174025_1174026del	NCBI36
NG_007460.2:g.38620_38621del , LRG_319:g.38620_38621del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.962_963del	ENSP00000490268.2:p.Pro321HisfsTer?
ENST00000585748.3:c.590_591del	ENSP00000477641.2:p.Pro197HisfsTer?
ENST00000585851.2:c.788_789del	ENSP00000467912.2:p.Pro263HisfsTer?
ENST00000326873.12:c.962_963del MANE Select	ENSP00000324856.6:p.Pro321HisfsTer?
ENST00000652231.1:c.962_963del	ENSP00000498804.1:p.Pro321HisfsTer?
ENST00000326873.11:c.962_963del	ENSP00000324856.6:p.Pro321HisfsTer?
ENST00000586243.5:c.962_963del	ENSP00000467240.2:p.Pro321HisfsTer?
ENST00000589152.5:n.1660_1661del
ENST00000591133.2:n.933_934del
NM_000455.4:c.962_963del , LRG_319t1:c.962_963del	NP_000446.1:p.Pro321HisfsTer?
XM_005259617.1:c.962_963del	XP_005259674.1:p.Pro321HisfsTer?
XM_005259618.3:c.962_963del	XP_005259675.1:p.Pro321HisfsTer?
XM_011528209.1:c.740_741del	XP_011526511.1:p.Pro247HisfsTer?
XR_936204.1:n.1738_1739del
XM_005259617.3:c.962_963del	XP_005259674.1:p.Pro321HisfsTer?
XM_011528209.2:c.740_741del	XP_011526511.1:p.Pro247HisfsTer?
XR_001753738.2:n.1768_1769del
XR_001753739.1:n.1768_1769del
XR_001753740.2:n.1738_1739del
NM_000455.5:c.962_963del MANE Select	NP_000446.1:p.Pro321HisfsTer?