Canonical Allele Identifier: CA2695196550

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220511_1220535delinsGCCGAGGGGGCCGAG , CM000681.2:g.1220511_1220535delinsGCCGAGGGGGCCGAG	GRCh38
NC_000019.9:g.1220510_1220534delinsGCCGAGGGGGCCGAG , CM000681.1:g.1220510_1220534delinsGCCGAGGGGGCCGAG	GRCh37
NC_000019.8:g.1171510_1171534delinsGCCGAGGGGGCCGAG	NCBI36
NG_007460.2:g.36105_36129delinsGCCGAGGGGGCCGAG , LRG_319:g.36105_36129delinsGCCGAGGGGGCCGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.597+6_597+30delinsGCCGAGGGGGCCGAG	ENSP00000490268.2:n.597+6_597+30delinsGCCGAGGGGGCCGAG
ENST00000585748.3:c.225+6_225+30delinsGCCGAGGGGGCCGAG	ENSP00000477641.2:n.225+6_225+30delinsGCCGAGGGGGCCGAG
ENST00000585851.2:c.423+6_423+30delinsGCCGAGGGGGCCGAG	ENSP00000467912.2:n.423+6_423+30delinsGCCGAGGGGGCCGAG
ENST00000326873.12:c.597+6_597+30delinsGCCGAGGGGGCCGAG MANE Select	ENSP00000324856.6:n.597+6_597+30delinsGCCGAGGGGGCCGAG
ENST00000652231.1:c.597+6_597+30delinsGCCGAGGGGGCCGAG	ENSP00000498804.1:n.597+6_597+30delinsGCCGAGGGGGCCGAG
ENST00000326873.11:c.597+6_597+30delinsGCCGAGGGGGCCGAG	ENSP00000324856.6:n.597+6_597+30delinsGCCGAGGGGGCCGAG
ENST00000585851.1:c.423+6_423+30delinsGCCGAGGGGGCCGAG	ENSP00000467912.1:n.423+6_423+30delinsGCCGAGGGGGCCGAG
ENST00000586243.5:c.597+6_597+30delinsGCCGAGGGGGCCGAG	ENSP00000467240.2:n.597+6_597+30delinsGCCGAGGGGGCCGAG
ENST00000586358.5:n.426_450delinsGCCGAGGGGGCCGAG
ENST00000589152.5:n.687+6_687+30delinsGCCGAGGGGGCCGAG
ENST00000591133.2:n.499_523delinsGCCGAGGGGGCCGAG
NM_000455.4:c.597+6_597+30delinsGCCGAGGGGGCCGAG , LRG_319t1:c.597+6_597+30delinsGCCGAGGGGGCCGAG	NP_000446.1:n.597+6_597+30delinsGCCGAGGGGGCCGAG
XM_005259617.1:c.597+6_597+30delinsGCCGAGGGGGCCGAG	XP_005259674.1:n.597+6_597+30delinsGCCGAGGGGGCCGAG
XM_005259618.3:c.597+6_597+30delinsGCCGAGGGGGCCGAG	XP_005259675.1:n.597+6_597+30delinsGCCGAGGGGGCCGAG
XM_011528209.1:c.375+6_375+30delinsGCCGAGGGGGCCGAG	XP_011526511.1:n.375+6_375+30delinsGCCGAGGGGGCCGAG
XR_936204.1:n.1222+6_1222+30delinsGCCGAGGGGGCCGAG
XM_005259617.3:c.597+6_597+30delinsGCCGAGGGGGCCGAG	XP_005259674.1:n.597+6_597+30delinsGCCGAGGGGGCCGAG
XM_011528209.2:c.375+6_375+30delinsGCCGAGGGGGCCGAG	XP_011526511.1:n.375+6_375+30delinsGCCGAGGGGGCCGAG
XR_001753738.2:n.1222+6_1222+30delinsGCCGAGGGGGCCGAG
XR_001753739.1:n.1222+6_1222+30delinsGCCGAGGGGGCCGAG
XR_001753740.2:n.1222+6_1222+30delinsGCCGAGGGGGCCGAG
NM_000455.5:c.597+6_597+30delinsGCCGAGGGGGCCGAG MANE Select	NP_000446.1:n.597+6_597+30delinsGCCGAGGGGGCCGAG