Canonical Allele Identifier: CA2317593749

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226574C= , CM000681.2:g.1226574C=	GRCh38
NC_000019.9:g.1226573C= , CM000681.1:g.1226573C=	GRCh37
NC_000019.8:g.1177573C=	NCBI36
NG_007460.2:g.42168C= , LRG_319:g.42168C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2830C=	ENSP00000490268.2:n.*2830C=
ENST00000585748.3:c.857C=	ENSP00000477641.2:p.Ala286=
ENST00000585851.2:c.1055C=	ENSP00000467912.2:p.Ala352=
ENST00000326873.12:c.1229C= MANE Select	ENSP00000324856.6:p.Ala410=
ENST00000326873.11:c.1229C=	ENSP00000324856.6:p.Ala410=
ENST00000585465.2:n.2962C=
ENST00000586243.5:c.1228C=	ENSP00000467240.2:p.Pro410=
ENST00000589152.5:n.1927C=
NM_000455.4:c.1229C= , LRG_319t1:c.1229C=	NP_000446.1:p.Ala410=
XM_005259617.1:c.1224C=	XP_005259674.1:p.Gly408=
XM_011528209.1:c.1002C=	XP_011526511.1:p.Gly334=
XM_005259617.3:c.1224C=	XP_005259674.1:p.Gly408=
XM_011528209.2:c.1002C=	XP_011526511.1:p.Gly334=
XR_001753738.2:n.2035C=
XR_001753740.2:n.2005C=
NM_000455.5:c.1229C= MANE Select	NP_000446.1:p.Ala410=