Canonical Allele Identifier: CA2317593747

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226572G= , CM000681.2:g.1226572G=	GRCh38
NC_000019.9:g.1226571G= , CM000681.1:g.1226571G=	GRCh37
NC_000019.8:g.1177571G=	NCBI36
NG_007460.2:g.42166G= , LRG_319:g.42166G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2828G=	ENSP00000490268.2:n.*2828G=
ENST00000585748.3:c.855G=	ENSP00000477641.2:p.Arg285=
ENST00000585851.2:c.1053G=	ENSP00000467912.2:p.Arg351=
ENST00000326873.12:c.1227G= MANE Select	ENSP00000324856.6:p.Arg409=
ENST00000326873.11:c.1227G=	ENSP00000324856.6:p.Arg409=
ENST00000585465.2:n.2960G=
ENST00000586243.5:c.1226G=	ENSP00000467240.2:p.Gly409=
ENST00000589152.5:n.1925G=
NM_000455.4:c.1227G= , LRG_319t1:c.1227G=	NP_000446.1:p.Arg409=
XM_005259617.1:c.1222G=	XP_005259674.1:p.Gly408=
XM_011528209.1:c.1000G=	XP_011526511.1:p.Gly334=
XM_005259617.3:c.1222G=	XP_005259674.1:p.Gly408=
XM_011528209.2:c.1000G=	XP_011526511.1:p.Gly334=
XR_001753738.2:n.2033G=
XR_001753740.2:n.2003G=
NM_000455.5:c.1227G= MANE Select	NP_000446.1:p.Arg409=