Canonical Allele Identifier: CA2317581430

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1206781T= , CM000681.2:g.1206781T=	GRCh38
NC_000019.9:g.1206780T= , CM000681.1:g.1206780T=	GRCh37
NC_000019.8:g.1157780T=	NCBI36
NG_007460.2:g.22375T= , LRG_319:g.22375T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.-133T=	ENSP00000490268.2:n.-133T=
ENST00000585748.3:c.-82-11636T=	ENSP00000477641.2:n.-82-11636T=
ENST00000326873.12:c.-133T= MANE Select	ENSP00000324856.6:n.-133T=
ENST00000652231.1:c.-133T=	ENSP00000498804.1:n.-133T=
ENST00000326873.11:c.-133T=	ENSP00000324856.6:n.-133T=
ENST00000585748.2:c.-82-11636T=	ENSP00000477641.1:n.-82-11636T=
ENST00000586243.5:c.-133T=	ENSP00000467240.2:n.-133T=
NM_000455.4:c.-133T= , LRG_319t1:c.-133T=	NP_000446.1:n.-133T=
XM_005259617.1:c.-133T=	XP_005259674.1:n.-133T=
XM_005259618.3:c.-133T=	XP_005259675.1:n.-133T=
XM_011528209.1:c.-486T=	XP_011526511.1:n.-486T=
XR_936204.1:n.493T=
XM_005259617.3:c.-133T=	XP_005259674.1:n.-133T=
XM_011528209.2:c.-486T=	XP_011526511.1:n.-486T=
XR_001753738.2:n.493T=
XR_001753739.1:n.493T=
XR_001753740.2:n.493T=
NM_000455.5:c.-133T= MANE Select	NP_000446.1:n.-133T=