Canonical Allele Identifier: CA2317591446

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1222996_1222997delinsAG , CM000681.2:g.1222996_1222997delinsAG	GRCh38
NC_000019.9:g.1222995_1222996delinsAG , CM000681.1:g.1222995_1222996delinsAG	GRCh37
NC_000019.8:g.1173995_1173996delinsAG	NCBI36
NG_007460.2:g.38590_38591delinsAG , LRG_319:g.38590_38591delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.932_933delinsAG	ENSP00000490268.2:p.Lys311=
ENST00000585748.3:c.560_561delinsAG	ENSP00000477641.2:p.Lys187=
ENST00000585851.2:c.758_759delinsAG	ENSP00000467912.2:p.Lys253=
ENST00000326873.12:c.932_933delinsAG MANE Select	ENSP00000324856.6:p.Lys311=
ENST00000652231.1:c.932_933delinsAG	ENSP00000498804.1:p.Lys311=
ENST00000326873.11:c.932_933delinsAG	ENSP00000324856.6:p.Lys311=
ENST00000586243.5:c.932_933delinsAG	ENSP00000467240.2:p.Lys311=
ENST00000589152.5:n.1630_1631delinsAG
ENST00000591133.2:n.903_904delinsAG
NM_000455.4:c.932_933delinsAG , LRG_319t1:c.932_933delinsAG	NP_000446.1:p.Lys311=
XM_005259617.1:c.932_933delinsAG	XP_005259674.1:p.Lys311=
XM_005259618.3:c.932_933delinsAG	XP_005259675.1:p.Lys311=
XM_011528209.1:c.710_711delinsAG	XP_011526511.1:p.Lys237=
XR_936204.1:n.1708_1709delinsAG
XM_005259617.3:c.932_933delinsAG	XP_005259674.1:p.Lys311=
XM_011528209.2:c.710_711delinsAG	XP_011526511.1:p.Lys237=
XR_001753738.2:n.1738_1739delinsAG
XR_001753739.1:n.1738_1739delinsAG
XR_001753740.2:n.1708_1709delinsAG
NM_000455.5:c.932_933delinsAG MANE Select	NP_000446.1:p.Lys311=