Canonical Allele Identifier: CA2317593771

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226601C= , CM000681.2:g.1226601C=	GRCh38
NC_000019.9:g.1226600C= , CM000681.1:g.1226600C=	GRCh37
NC_000019.8:g.1177600C=	NCBI36
NG_007460.2:g.42195C= , LRG_319:g.42195C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2857C=	ENSP00000490268.2:n.*2857C=
ENST00000585748.3:c.884C=	ENSP00000477641.2:p.Ser295=
ENST00000585851.2:c.1082C=	ENSP00000467912.2:p.Ser361=
ENST00000326873.12:c.1256C= MANE Select	ENSP00000324856.6:p.Ser419=
ENST00000326873.11:c.1256C=	ENSP00000324856.6:p.Ser419=
ENST00000585465.2:n.2989C=
ENST00000586243.5:c.1255-2C=	ENSP00000467240.2:n.1255-2C=
ENST00000589152.5:n.1954C=
NM_000455.4:c.1256C= , LRG_319t1:c.1256C=	NP_000446.1:p.Ser419=
XM_005259617.1:c.1251C=	XP_005259674.1:p.Leu417=
XM_011528209.1:c.1029C=	XP_011526511.1:p.Leu343=
XM_005259617.3:c.1251C=	XP_005259674.1:p.Leu417=
XM_011528209.2:c.1029C=	XP_011526511.1:p.Leu343=
XR_001753738.2:n.2062C=
XR_001753740.2:n.2032C=
NM_000455.5:c.1256C= MANE Select	NP_000446.1:p.Ser419=