Canonical Allele Identifier: CA2317593789

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226618C= , CM000681.2:g.1226618C=	GRCh38
NC_000019.9:g.1226617C= , CM000681.1:g.1226617C=	GRCh37
NC_000019.8:g.1177617C=	NCBI36
NG_007460.2:g.42212C= , LRG_319:g.42212C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2874C=	ENSP00000490268.2:n.*2874C=
ENST00000585748.3:c.901C=	ENSP00000477641.2:p.Arg301=
ENST00000585851.2:c.1099C=	ENSP00000467912.2:p.Arg367=
ENST00000326873.12:c.1273C= MANE Select	ENSP00000324856.6:p.Arg425=
ENST00000326873.11:c.1273C=	ENSP00000324856.6:p.Arg425=
ENST00000585465.2:n.3006C=
ENST00000586243.5:c.1270C=	ENSP00000467240.2:p.Arg424=
ENST00000589152.5:n.1971C=
NM_000455.4:c.1273C= , LRG_319t1:c.1273C=	NP_000446.1:p.Arg425=
XM_005259617.1:c.1268C=	XP_005259674.1:p.Pro423=
XM_011528209.1:c.1046C=	XP_011526511.1:p.Pro349=
XM_005259617.3:c.1268C=	XP_005259674.1:p.Pro423=
XM_011528209.2:c.1046C=	XP_011526511.1:p.Pro349=
XR_001753738.2:n.2079C=
XR_001753740.2:n.2049C=
NM_000455.5:c.1273C= MANE Select	NP_000446.1:p.Arg425=