Canonical Allele Identifier: CA2317589744

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220389_1220397delinsATTGACGGC , CM000681.2:g.1220389_1220397delinsATTGACGGC	GRCh38
NC_000019.9:g.1220388_1220396delinsATTGACGGC , CM000681.1:g.1220388_1220396delinsATTGACGGC	GRCh37
NC_000019.8:g.1171388_1171396delinsATTGACGGC	NCBI36
NG_007460.2:g.35983_35991delinsATTGACGGC , LRG_319:g.35983_35991delinsATTGACGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.481_489delinsATTGACGGC	ENSP00000490268.2:p.Ile161=
ENST00000585748.3:c.109_117delinsATTGACGGC	ENSP00000477641.2:p.Ile37=
ENST00000585851.2:c.307_315delinsATTGACGGC	ENSP00000467912.2:p.Ile103=
ENST00000326873.12:c.481_489delinsATTGACGGC MANE Select	ENSP00000324856.6:p.Ile161=
ENST00000652231.1:c.481_489delinsATTGACGGC	ENSP00000498804.1:p.Ile161=
ENST00000326873.11:c.481_489delinsATTGACGGC	ENSP00000324856.6:p.Ile161=
ENST00000585851.1:c.307_315delinsATTGACGGC	ENSP00000467912.1:p.Ile103=
ENST00000586243.5:c.481_489delinsATTGACGGC	ENSP00000467240.2:p.Ile161=
ENST00000586358.5:n.304_312delinsATTGACGGC
ENST00000589152.5:n.571_579delinsATTGACGGC
ENST00000591133.2:n.377_385delinsATTGACGGC
NM_000455.4:c.481_489delinsATTGACGGC , LRG_319t1:c.481_489delinsATTGACGGC	NP_000446.1:p.Ile161=
XM_005259617.1:c.481_489delinsATTGACGGC	XP_005259674.1:p.Ile161=
XM_005259618.3:c.481_489delinsATTGACGGC	XP_005259675.1:p.Ile161=
XM_011528209.1:c.259_267delinsATTGACGGC	XP_011526511.1:p.Ile87=
XR_936204.1:n.1106_1114delinsATTGACGGC
XM_005259617.3:c.481_489delinsATTGACGGC	XP_005259674.1:p.Ile161=
XM_011528209.2:c.259_267delinsATTGACGGC	XP_011526511.1:p.Ile87=
XR_001753738.2:n.1106_1114delinsATTGACGGC
XR_001753739.1:n.1106_1114delinsATTGACGGC
XR_001753740.2:n.1106_1114delinsATTGACGGC
NM_000455.5:c.481_489delinsATTGACGGC MANE Select	NP_000446.1:p.Ile161=