Canonical Allele Identifier: CA2317588557

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218482_1218483delinsAC , CM000681.2:g.1218482_1218483delinsAC	GRCh38
NC_000019.9:g.1218481_1218482delinsAC , CM000681.1:g.1218481_1218482delinsAC	GRCh37
NC_000019.8:g.1169481_1169482delinsAC	NCBI36
NG_007460.2:g.34076_34077delinsAC , LRG_319:g.34076_34077delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.356_357delinsAC	ENSP00000490268.2:p.Asn119=
ENST00000585748.3:c.-17_-16delinsAC	ENSP00000477641.2:n.-17_-16delinsAC
ENST00000585851.2:c.291-1891_291-1890delinsAC	ENSP00000467912.2:n.291-1891_291-1890delinsAC
ENST00000326873.12:c.356_357delinsAC MANE Select	ENSP00000324856.6:p.Asn119=
ENST00000652231.1:c.356_357delinsAC	ENSP00000498804.1:p.Asn119=
ENST00000326873.11:c.356_357delinsAC	ENSP00000324856.6:p.Asn119=
ENST00000585748.2:c.-17_-16delinsAC	ENSP00000477641.1:n.-17_-16delinsAC
ENST00000585851.1:c.291-1891_291-1890delinsAC	ENSP00000467912.1:n.291-1891_291-1890delinsAC
ENST00000586243.5:c.356_357delinsAC	ENSP00000467240.2:p.Asn119=
ENST00000586358.5:n.179_180delinsAC
ENST00000589152.5:n.446_447delinsAC
ENST00000593219.5:c.*181_*182delinsAC	ENSP00000466610.1:n.*181_*182delinsAC
NM_000455.4:c.356_357delinsAC , LRG_319t1:c.356_357delinsAC	NP_000446.1:p.Asn119=
XM_005259617.1:c.356_357delinsAC	XP_005259674.1:p.Asn119=
XM_005259618.3:c.356_357delinsAC	XP_005259675.1:p.Asn119=
XM_011528209.1:c.134_135delinsAC	XP_011526511.1:p.Asn45=
XR_936204.1:n.981_982delinsAC
XM_005259617.3:c.356_357delinsAC	XP_005259674.1:p.Asn119=
XM_011528209.2:c.134_135delinsAC	XP_011526511.1:p.Asn45=
XR_001753738.2:n.981_982delinsAC
XR_001753739.1:n.981_982delinsAC
XR_001753740.2:n.981_982delinsAC
NM_000455.5:c.356_357delinsAC MANE Select	NP_000446.1:p.Asn119=