Canonical Allele Identifier: CA2317591566

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1223140_1223143delinsACAT , CM000681.2:g.1223140_1223143delinsACAT	GRCh38
NC_000019.9:g.1223139_1223142delinsACAT , CM000681.1:g.1223139_1223142delinsACAT	GRCh37
NC_000019.8:g.1174139_1174142delinsACAT	NCBI36
NG_007460.2:g.38734_38737delinsACAT , LRG_319:g.38734_38737delinsACAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.1076_1079delinsACAT	ENSP00000490268.2:p.Asp359=
ENST00000585748.3:c.704_707delinsACAT	ENSP00000477641.2:p.Asp235=
ENST00000585851.2:c.902_905delinsACAT	ENSP00000467912.2:p.Asp301=
ENST00000326873.12:c.1076_1079delinsACAT MANE Select	ENSP00000324856.6:p.Asp359=
ENST00000652231.1:c.1076_1079delinsACAT	ENSP00000498804.1:p.Asp359=
ENST00000326873.11:c.1076_1079delinsACAT	ENSP00000324856.6:p.Asp359=
ENST00000586243.5:c.1076_1079delinsACAT	ENSP00000467240.2:p.Asp359=
ENST00000589152.5:n.1774_1777delinsACAT
NM_000455.4:c.1076_1079delinsACAT , LRG_319t1:c.1076_1079delinsACAT	NP_000446.1:p.Asp359=
XM_005259617.1:c.1076_1079delinsACAT	XP_005259674.1:p.Asp359=
XM_005259618.3:c.1076_1079delinsACAT	XP_005259675.1:p.Asp359=
XM_011528209.1:c.854_857delinsACAT	XP_011526511.1:p.Asp285=
XR_936204.1:n.1852_1855delinsACAT
XM_005259617.3:c.1076_1079delinsACAT	XP_005259674.1:p.Asp359=
XM_011528209.2:c.854_857delinsACAT	XP_011526511.1:p.Asp285=
XR_001753738.2:n.1882_1885delinsACAT
XR_001753739.1:n.1882_1885delinsACAT
XR_001753740.2:n.1852_1855delinsACAT
NM_000455.5:c.1076_1079delinsACAT MANE Select	NP_000446.1:p.Asp359=