Canonical Allele Identifier: CA2317593776

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226604C= , CM000681.2:g.1226604C=	GRCh38
NC_000019.9:g.1226603C= , CM000681.1:g.1226603C=	GRCh37
NC_000019.8:g.1177603C=	NCBI36
NG_007460.2:g.42198C= , LRG_319:g.42198C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2860C=	ENSP00000490268.2:n.*2860C=
ENST00000585748.3:c.887C=	ENSP00000477641.2:p.Ala296=
ENST00000585851.2:c.1085C=	ENSP00000467912.2:p.Ala362=
ENST00000326873.12:c.1259C= MANE Select	ENSP00000324856.6:p.Ala420=
ENST00000326873.11:c.1259C=	ENSP00000324856.6:p.Ala420=
ENST00000585465.2:n.2992C=
ENST00000586243.5:c.1256C=	ENSP00000467240.2:p.Ala419=
ENST00000589152.5:n.1957C=
NM_000455.4:c.1259C= , LRG_319t1:c.1259C=	NP_000446.1:p.Ala420=
XM_005259617.1:c.1254C=	XP_005259674.1:p.Arg418=
XM_011528209.1:c.1032C=	XP_011526511.1:p.Arg344=
XM_005259617.3:c.1254C=	XP_005259674.1:p.Arg418=
XM_011528209.2:c.1032C=	XP_011526511.1:p.Arg344=
XR_001753738.2:n.2065C=
XR_001753740.2:n.2035C=
NM_000455.5:c.1259C= MANE Select	NP_000446.1:p.Ala420=