Canonical Allele Identifier: CA2695227862

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1207109_1207123del , CM000681.2:g.1207109_1207123del	GRCh38
NC_000019.9:g.1207108_1207122del , CM000681.1:g.1207108_1207122del	GRCh37
NC_000019.8:g.1158108_1158122del	NCBI36
NG_007460.2:g.22703_22717del , LRG_319:g.22703_22717del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.196_210del	ENSP00000490268.2:p.Val66_Glu70del
ENST00000585748.3:c.-82-11308_-82-11294del	ENSP00000477641.2:n.-82-11308_-82-11294del
ENST00000585851.2:c.196_210del	ENSP00000467912.2:p.Val66_Glu70del
ENST00000326873.12:c.196_210del MANE Select	ENSP00000324856.6:p.Val66_Glu70del
ENST00000652231.1:c.196_210del	ENSP00000498804.1:p.Val66_Glu70del
ENST00000326873.11:c.196_210del	ENSP00000324856.6:p.Val66_Glu70del
ENST00000585748.2:c.-82-11308_-82-11294del	ENSP00000477641.1:n.-82-11308_-82-11294del
ENST00000585851.1:c.196_210del	ENSP00000467912.1:p.Val66_Glu70del
ENST00000586243.5:c.196_210del	ENSP00000467240.2:p.Val66_Glu70del
ENST00000586358.5:n.19_33del
ENST00000589152.5:n.286_300del
ENST00000593219.5:c.196_210del	ENSP00000466610.1:p.Val66_Glu70del
NM_000455.4:c.196_210del , LRG_319t1:c.196_210del	NP_000446.1:p.Val66_Glu70del
XM_005259617.1:c.196_210del	XP_005259674.1:p.Val66_Glu70del
XM_005259618.3:c.196_210del	XP_005259675.1:p.Val66_Glu70del
XM_011528209.1:c.-158_-144del	XP_011526511.1:n.-158_-144del
XR_936204.1:n.821_835del
XM_005259617.3:c.196_210del	XP_005259674.1:p.Val66_Glu70del
XM_011528209.2:c.-158_-144del	XP_011526511.1:n.-158_-144del
XR_001753738.2:n.821_835del
XR_001753739.1:n.821_835del
XR_001753740.2:n.821_835del
NM_000455.5:c.196_210del MANE Select	NP_000446.1:p.Val66_Glu70del