Canonical Allele Identifier: CA2317590775

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1221975_1221976delinsAG , CM000681.2:g.1221975_1221976delinsAG	GRCh38
NC_000019.9:g.1221974_1221975delinsAG , CM000681.1:g.1221974_1221975delinsAG	GRCh37
NC_000019.8:g.1172974_1172975delinsAG	NCBI36
NG_007460.2:g.37569_37570delinsAG , LRG_319:g.37569_37570delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.889_890delinsAG	ENSP00000490268.2:p.Arg297=
ENST00000585748.3:c.517_518delinsAG	ENSP00000477641.2:p.Arg173=
ENST00000585851.2:c.715_716delinsAG	ENSP00000467912.2:p.Arg239=
ENST00000326873.12:c.889_890delinsAG MANE Select	ENSP00000324856.6:p.Arg297=
ENST00000652231.1:c.889_890delinsAG	ENSP00000498804.1:p.Arg297=
ENST00000326873.11:c.889_890delinsAG	ENSP00000324856.6:p.Arg297=
ENST00000586243.5:c.889_890delinsAG	ENSP00000467240.2:p.Arg297=
ENST00000589152.5:n.1587_1588delinsAG
ENST00000591133.2:n.860_861delinsAG
NM_000455.4:c.889_890delinsAG , LRG_319t1:c.889_890delinsAG	NP_000446.1:p.Arg297=
XM_005259617.1:c.889_890delinsAG	XP_005259674.1:p.Arg297=
XM_005259618.3:c.889_890delinsAG	XP_005259675.1:p.Arg297=
XM_011528209.1:c.667_668delinsAG	XP_011526511.1:p.Arg223=
XR_936204.1:n.1665_1666delinsAG
XM_005259617.3:c.889_890delinsAG	XP_005259674.1:p.Arg297=
XM_011528209.2:c.667_668delinsAG	XP_011526511.1:p.Arg223=
XR_001753738.2:n.1695_1696delinsAG
XR_001753739.1:n.1695_1696delinsAG
XR_001753740.2:n.1665_1666delinsAG
NM_000455.5:c.889_890delinsAG MANE Select	NP_000446.1:p.Arg297=