Canonical Allele Identifier: CA2695227762

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218447_1218452del , CM000681.2:g.1218447_1218452del	GRCh38
NC_000019.9:g.1218446_1218451del , CM000681.1:g.1218446_1218451del	GRCh37
NC_000019.8:g.1169446_1169451del	NCBI36
NG_007460.2:g.34041_34046del , LRG_319:g.34041_34046del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.321_326del	ENSP00000490268.2:p.Lys108_Asn109del
ENST00000585748.3:c.-52_-47del	ENSP00000477641.2:n.-52_-47del
ENST00000585851.2:c.291-1926_291-1921del	ENSP00000467912.2:n.291-1926_291-1921del
ENST00000326873.12:c.321_326del MANE Select	ENSP00000324856.6:p.Lys108_Asn109del
ENST00000652231.1:c.321_326del	ENSP00000498804.1:p.Lys108_Asn109del
ENST00000326873.11:c.321_326del	ENSP00000324856.6:p.Lys108_Asn109del
ENST00000585748.2:c.-52_-47del	ENSP00000477641.1:n.-52_-47del
ENST00000585851.1:c.291-1926_291-1921del	ENSP00000467912.1:n.291-1926_291-1921del
ENST00000586243.5:c.321_326del	ENSP00000467240.2:p.Lys108_Asn109del
ENST00000586358.5:n.144_149del
ENST00000589152.5:n.411_416del
ENST00000593219.5:c.*146_*151del	ENSP00000466610.1:n.*146_*151del
NM_000455.4:c.321_326del , LRG_319t1:c.321_326del	NP_000446.1:p.Lys108_Asn109del
XM_005259617.1:c.321_326del	XP_005259674.1:p.Lys108_Asn109del
XM_005259618.3:c.321_326del	XP_005259675.1:p.Lys108_Asn109del
XM_011528209.1:c.99_104del	XP_011526511.1:p.Lys34_Asn35del
XR_936204.1:n.946_951del
XM_005259617.3:c.321_326del	XP_005259674.1:p.Lys108_Asn109del
XM_011528209.2:c.99_104del	XP_011526511.1:p.Lys34_Asn35del
XR_001753738.2:n.946_951del
XR_001753739.1:n.946_951del
XR_001753740.2:n.946_951del
NM_000455.5:c.321_326del MANE Select	NP_000446.1:p.Lys108_Asn109del