Canonical Allele Identifier: CA2317593843

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226683G= , CM000681.2:g.1226683G=	GRCh38
NC_000019.9:g.1226682G= , CM000681.1:g.1226682G=	GRCh37
NC_000019.8:g.1177682G=	NCBI36
NG_007460.2:g.42277G= , LRG_319:g.42277G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2919+20G=	ENSP00000490268.2:n.*2919+20G=
ENST00000585748.3:c.*16+20G=	ENSP00000477641.2:n.*16+20G=
ENST00000585851.2:c.*16+20G=	ENSP00000467912.2:n.*16+20G=
ENST00000326873.12:c.*16+20G= MANE Select	ENSP00000324856.6:n.*16+20G=
ENST00000326873.11:c.*16+20G=	ENSP00000324856.6:n.*16+20G=
ENST00000585465.2:n.3051+20G=
ENST00000586243.5:c.*16+20G=	ENSP00000467240.2:n.*16+20G=
ENST00000589152.5:n.2036G=
NM_000455.4:c.*16+20G= , LRG_319t1:c.*16+20G=	NP_000446.1:n.*16+20G=
XM_005259617.1:c.1313+20G=	XP_005259674.1:n.1313+20G=
XM_011528209.1:c.1091+20G=	XP_011526511.1:n.1091+20G=
XM_005259617.3:c.1313+20G=	XP_005259674.1:n.1313+20G=
XM_011528209.2:c.1091+20G=	XP_011526511.1:n.1091+20G=
XR_001753738.2:n.2124+20G=
XR_001753740.2:n.2094+20G=
NM_000455.5:c.*16+20G= MANE Select	NP_000446.1:n.*16+20G=