Canonical Allele Identifier: CA2317593791

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226621C= , CM000681.2:g.1226621C=	GRCh38
NC_000019.9:g.1226620C= , CM000681.1:g.1226620C=	GRCh37
NC_000019.8:g.1177620C=	NCBI36
NG_007460.2:g.42215C= , LRG_319:g.42215C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2877C=	ENSP00000490268.2:n.*2877C=
ENST00000585748.3:c.904C=	ENSP00000477641.2:p.Arg302=
ENST00000585851.2:c.1102C=	ENSP00000467912.2:p.Arg368=
ENST00000326873.12:c.1276C= MANE Select	ENSP00000324856.6:p.Arg426=
ENST00000326873.11:c.1276C=	ENSP00000324856.6:p.Arg426=
ENST00000585465.2:n.3009C=
ENST00000586243.5:c.1273C=	ENSP00000467240.2:p.Arg425=
ENST00000589152.5:n.1974C=
NM_000455.4:c.1276C= , LRG_319t1:c.1276C=	NP_000446.1:p.Arg426=
XM_005259617.1:c.1271C=	XP_005259674.1:p.Pro424=
XM_011528209.1:c.1049C=	XP_011526511.1:p.Pro350=
XM_005259617.3:c.1271C=	XP_005259674.1:p.Pro424=
XM_011528209.2:c.1049C=	XP_011526511.1:p.Pro350=
XR_001753738.2:n.2082C=
XR_001753740.2:n.2052C=
NM_000455.5:c.1276C= MANE Select	NP_000446.1:p.Arg426=