Canonical Allele Identifier: CA2695227939

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1223053_1223061del , CM000681.2:g.1223053_1223061del	GRCh38
NC_000019.9:g.1223052_1223060del , CM000681.1:g.1223052_1223060del	GRCh37
NC_000019.8:g.1174052_1174060del	NCBI36
NG_007460.2:g.38647_38655del , LRG_319:g.38647_38655del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.989_997del	ENSP00000490268.2:p.Asp330_Arg333delinsGly
ENST00000585748.3:c.617_625del	ENSP00000477641.2:p.Asp206_Arg209delinsGly
ENST00000585851.2:c.815_823del	ENSP00000467912.2:p.Asp272_Arg275delinsGly
ENST00000326873.12:c.989_997del MANE Select	ENSP00000324856.6:p.Asp330_Arg333delinsGly
ENST00000652231.1:c.989_997del	ENSP00000498804.1:p.Asp330_Arg333delinsGly
ENST00000326873.11:c.989_997del	ENSP00000324856.6:p.Asp330_Arg333delinsGly
ENST00000586243.5:c.989_997del	ENSP00000467240.2:p.Asp330_Arg333delinsGly
ENST00000589152.5:n.1687_1695del
ENST00000591133.2:n.960_968del
NM_000455.4:c.989_997del , LRG_319t1:c.989_997del	NP_000446.1:p.Asp330_Arg333delinsGly
XM_005259617.1:c.989_997del	XP_005259674.1:p.Asp330_Arg333delinsGly
XM_005259618.3:c.989_997del	XP_005259675.1:p.Asp330_Arg333delinsGly
XM_011528209.1:c.767_775del	XP_011526511.1:p.Asp256_Arg259delinsGly
XR_936204.1:n.1765_1773del
XM_005259617.3:c.989_997del	XP_005259674.1:p.Asp330_Arg333delinsGly
XM_011528209.2:c.767_775del	XP_011526511.1:p.Asp256_Arg259delinsGly
XR_001753738.2:n.1795_1803del
XR_001753739.1:n.1795_1803del
XR_001753740.2:n.1765_1773del
NM_000455.5:c.989_997del MANE Select	NP_000446.1:p.Asp330_Arg333delinsGly