Canonical Allele Identifier: CA2317593745

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226571G= , CM000681.2:g.1226571G=	GRCh38
NC_000019.9:g.1226570G= , CM000681.1:g.1226570G=	GRCh37
NC_000019.8:g.1177570G=	NCBI36
NG_007460.2:g.42165G= , LRG_319:g.42165G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2827G=	ENSP00000490268.2:n.*2827G=
ENST00000585748.3:c.854G=	ENSP00000477641.2:p.Arg285=
ENST00000585851.2:c.1052G=	ENSP00000467912.2:p.Arg351=
ENST00000326873.12:c.1226G= MANE Select	ENSP00000324856.6:p.Arg409=
ENST00000326873.11:c.1226G=	ENSP00000324856.6:p.Arg409=
ENST00000585465.2:n.2959G=
ENST00000586243.5:c.1225G=	ENSP00000467240.2:p.Gly409=
ENST00000589152.5:n.1924G=
NM_000455.4:c.1226G= , LRG_319t1:c.1226G=	NP_000446.1:p.Arg409=
XM_005259617.1:c.1221G=	XP_005259674.1:p.Pro407=
XM_011528209.1:c.999G=	XP_011526511.1:p.Pro333=
XM_005259617.3:c.1221G=	XP_005259674.1:p.Pro407=
XM_011528209.2:c.999G=	XP_011526511.1:p.Pro333=
XR_001753738.2:n.2032G=
XR_001753740.2:n.2002G=
NM_000455.5:c.1226G= MANE Select	NP_000446.1:p.Arg409=