Canonical Allele Identifier: CA2317593678

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226492C= , CM000681.2:g.1226492C=	GRCh38
NC_000019.9:g.1226491C= , CM000681.1:g.1226491C=	GRCh37
NC_000019.8:g.1177491C=	NCBI36
NG_007460.2:g.42086C= , LRG_319:g.42086C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000455.5:c.1147C= MANE Select	NP_000446.1:p.Arg383=
ENST00000326873.12:c.1147C= MANE Select	ENSP00000324856.6:p.Arg383=
NM_000455.4:c.1147C= , LRG_319t1:c.1147C=	NP_000446.1:p.Arg383=
ENST00000326873.11:c.1147C=	ENSP00000324856.6:p.Arg383=
ENST00000585465.2:n.2880C=
ENST00000585465.3:c.*2748C=	ENSP00000490268.2:n.*2748C=
ENST00000585748.3:c.775C=	ENSP00000477641.2:p.Arg259=
ENST00000585851.2:c.973C=	ENSP00000467912.2:p.Arg325=
ENST00000586243.5:c.1147C=	ENSP00000467240.2:p.Arg383=
ENST00000589152.5:n.1845C=
XM_005259617.1:c.1142C=	XP_005259674.1:p.Ala381=
XM_005259617.3:c.1142C=	XP_005259674.1:p.Ala381=
XM_011528209.1:c.920C=	XP_011526511.1:p.Ala307=
XM_011528209.2:c.920C=	XP_011526511.1:p.Ala307=
XR_001753738.2:n.1953C=
XR_001753740.2:n.1923C=