Canonical Allele Identifier: CA2317591489

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1223043_1223045delinsGAC , CM000681.2:g.1223043_1223045delinsGAC	GRCh38
NC_000019.9:g.1223042_1223044delinsGAC , CM000681.1:g.1223042_1223044delinsGAC	GRCh37
NC_000019.8:g.1174042_1174044delinsGAC	NCBI36
NG_007460.2:g.38637_38639delinsGAC , LRG_319:g.38637_38639delinsGAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.979_981delinsGAC	ENSP00000490268.2:p.Asp327=
ENST00000585748.3:c.607_609delinsGAC	ENSP00000477641.2:p.Asp203=
ENST00000585851.2:c.805_807delinsGAC	ENSP00000467912.2:p.Asp269=
ENST00000326873.12:c.979_981delinsGAC MANE Select	ENSP00000324856.6:p.Asp327=
ENST00000652231.1:c.979_981delinsGAC	ENSP00000498804.1:p.Asp327=
ENST00000326873.11:c.979_981delinsGAC	ENSP00000324856.6:p.Asp327=
ENST00000586243.5:c.979_981delinsGAC	ENSP00000467240.2:p.Asp327=
ENST00000589152.5:n.1677_1679delinsGAC
ENST00000591133.2:n.950_952delinsGAC
NM_000455.4:c.979_981delinsGAC , LRG_319t1:c.979_981delinsGAC	NP_000446.1:p.Asp327=
XM_005259617.1:c.979_981delinsGAC	XP_005259674.1:p.Asp327=
XM_005259618.3:c.979_981delinsGAC	XP_005259675.1:p.Asp327=
XM_011528209.1:c.757_759delinsGAC	XP_011526511.1:p.Asp253=
XR_936204.1:n.1755_1757delinsGAC
XM_005259617.3:c.979_981delinsGAC	XP_005259674.1:p.Asp327=
XM_011528209.2:c.757_759delinsGAC	XP_011526511.1:p.Asp253=
XR_001753738.2:n.1785_1787delinsGAC
XR_001753739.1:n.1785_1787delinsGAC
XR_001753740.2:n.1755_1757delinsGAC
NM_000455.5:c.979_981delinsGAC MANE Select	NP_000446.1:p.Asp327=