Canonical Allele Identifier: CA2317589776

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220438T= , CM000681.2:g.1220438T=	GRCh38
NC_000019.9:g.1220437T= , CM000681.1:g.1220437T=	GRCh37
NC_000019.8:g.1171437T=	NCBI36
NG_007460.2:g.36032T= , LRG_319:g.36032T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000455.5:c.530T= MANE Select	NP_000446.1:p.Ile177=
ENST00000326873.12:c.530T= MANE Select	ENSP00000324856.6:p.Ile177=
NM_000455.4:c.530T= , LRG_319t1:c.530T=	NP_000446.1:p.Ile177=
ENST00000326873.11:c.530T=	ENSP00000324856.6:p.Ile177=
ENST00000585465.3:c.530T=	ENSP00000490268.2:p.Ile177=
ENST00000585748.3:c.158T=	ENSP00000477641.2:p.Ile53=
ENST00000585851.1:c.356T=	ENSP00000467912.1:p.Ile119=
ENST00000585851.2:c.356T=	ENSP00000467912.2:p.Ile119=
ENST00000586243.5:c.530T=	ENSP00000467240.2:p.Ile177=
ENST00000586358.5:n.353T=
ENST00000589152.5:n.620T=
ENST00000591133.2:n.426T=
ENST00000652231.1:c.530T=	ENSP00000498804.1:p.Ile177=
XM_005259617.1:c.530T=	XP_005259674.1:p.Ile177=
XM_005259617.3:c.530T=	XP_005259674.1:p.Ile177=
XM_005259618.3:c.530T=	XP_005259675.1:p.Ile177=
XM_011528209.1:c.308T=	XP_011526511.1:p.Ile103=
XM_011528209.2:c.308T=	XP_011526511.1:p.Ile103=
XR_001753738.2:n.1155T=
XR_001753739.1:n.1155T=
XR_001753740.2:n.1155T=
XR_936204.1:n.1155T=