Canonical Allele Identifier: CA2317593727

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226548C= , CM000681.2:g.1226548C=	GRCh38
NC_000019.9:g.1226547C= , CM000681.1:g.1226547C=	GRCh37
NC_000019.8:g.1177547C=	NCBI36
NG_007460.2:g.42142C= , LRG_319:g.42142C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.*2804C=	ENSP00000490268.2:n.*2804C=
ENST00000585748.3:c.831C=	ENSP00000477641.2:p.Ser277=
ENST00000585851.2:c.1029C=	ENSP00000467912.2:p.Ser343=
ENST00000326873.12:c.1203C= MANE Select	ENSP00000324856.6:p.Ser401=
ENST00000326873.11:c.1203C=	ENSP00000324856.6:p.Ser401=
ENST00000585465.2:n.2936C=
ENST00000586243.5:c.1203C=	ENSP00000467240.2:p.Ser401=
ENST00000589152.5:n.1901C=
NM_000455.4:c.1203C= , LRG_319t1:c.1203C=	NP_000446.1:p.Ser401=
XM_005259617.1:c.1198C=	XP_005259674.1:p.His400=
XM_011528209.1:c.976C=	XP_011526511.1:p.His326=
XM_005259617.3:c.1198C=	XP_005259674.1:p.His400=
XM_011528209.2:c.976C=	XP_011526511.1:p.His326=
XR_001753738.2:n.2009C=
XR_001753740.2:n.1979C=
NM_000455.5:c.1203C= MANE Select	NP_000446.1:p.Ser401=