Canonical Allele Identifier: CA2317593667

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226481A= , CM000681.2:g.1226481A=	GRCh38
NC_000019.9:g.1226480A= , CM000681.1:g.1226480A=	GRCh37
NC_000019.8:g.1177480A=	NCBI36
NG_007460.2:g.42075A= , LRG_319:g.42075A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2737A=	ENSP00000490268.2:n.*2737A=
ENST00000585748.3:c.764A=	ENSP00000477641.2:p.His255=
ENST00000585851.2:c.962A=	ENSP00000467912.2:p.His321=
ENST00000326873.12:c.1136A= MANE Select	ENSP00000324856.6:p.His379=
ENST00000326873.11:c.1136A=	ENSP00000324856.6:p.His379=
ENST00000585465.2:n.2869A=
ENST00000586243.5:c.1136A=	ENSP00000467240.2:p.His379=
ENST00000589152.5:n.1834A=
NM_000455.4:c.1136A= , LRG_319t1:c.1136A=	NP_000446.1:p.His379=
XM_005259617.1:c.1131A=	XP_005259674.1:p.Ser377=
XM_011528209.1:c.909A=	XP_011526511.1:p.Ser303=
XM_005259617.3:c.1131A=	XP_005259674.1:p.Ser377=
XM_011528209.2:c.909A=	XP_011526511.1:p.Ser303=
XR_001753738.2:n.1942A=
XR_001753740.2:n.1912A=
NM_000455.5:c.1136A= MANE Select	NP_000446.1:p.His379=