Canonical Allele Identifier: CA2317591370

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1222885G= , CM000681.2:g.1222885G=	GRCh38
NC_000019.9:g.1222884G= , CM000681.1:g.1222884G=	GRCh37
NC_000019.8:g.1173884G=	NCBI36
NG_007460.2:g.38479G= , LRG_319:g.38479G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.921-100G=	ENSP00000490268.2:n.921-100G=
ENST00000585748.3:c.549-100G=	ENSP00000477641.2:n.549-100G=
ENST00000585851.2:c.747-100G=	ENSP00000467912.2:n.747-100G=
ENST00000326873.12:c.921-100G= MANE Select	ENSP00000324856.6:n.921-100G=
ENST00000652231.1:c.921-100G=	ENSP00000498804.1:n.921-100G=
ENST00000326873.11:c.921-100G=	ENSP00000324856.6:n.921-100G=
ENST00000586243.5:c.921-100G=	ENSP00000467240.2:n.921-100G=
ENST00000589152.5:n.1619-100G=
ENST00000591133.2:n.892-100G=
NM_000455.4:c.921-100G= , LRG_319t1:c.921-100G=	NP_000446.1:n.921-100G=
XM_005259617.1:c.921-100G=	XP_005259674.1:n.921-100G=
XM_005259618.3:c.921-100G=	XP_005259675.1:n.921-100G=
XM_011528209.1:c.699-100G=	XP_011526511.1:n.699-100G=
XR_936204.1:n.1697-100G=
XM_005259617.3:c.921-100G=	XP_005259674.1:n.921-100G=
XM_011528209.2:c.699-100G=	XP_011526511.1:n.699-100G=
XR_001753738.2:n.1727-100G=
XR_001753739.1:n.1727-100G=
XR_001753740.2:n.1697-100G=
NM_000455.5:c.921-100G= MANE Select	NP_000446.1:n.921-100G=