Canonical Allele Identifier: CA2317593648

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226458G= , CM000681.2:g.1226458G=	GRCh38
NC_000019.9:g.1226457G= , CM000681.1:g.1226457G=	GRCh37
NC_000019.8:g.1177457G=	NCBI36
NG_007460.2:g.42052G= , LRG_319:g.42052G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2714G=	ENSP00000490268.2:n.*2714G=
ENST00000585748.3:c.741G=	ENSP00000477641.2:p.Gln247=
ENST00000585851.2:c.939G=	ENSP00000467912.2:p.Gln313=
ENST00000326873.12:c.1113G= MANE Select	ENSP00000324856.6:p.Gln371=
ENST00000326873.11:c.1113G=	ENSP00000324856.6:p.Gln371=
ENST00000585465.2:n.2846G=
ENST00000586243.5:c.1113G=	ENSP00000467240.2:p.Gln371=
ENST00000589152.5:n.1811G=
NM_000455.4:c.1113G= , LRG_319t1:c.1113G=	NP_000446.1:p.Gln371=
XM_005259617.1:c.1109-1G=	XP_005259674.1:n.1109-1G=
XM_011528209.1:c.887-1G=	XP_011526511.1:n.887-1G=
XM_005259617.3:c.1109-1G=	XP_005259674.1:n.1109-1G=
XM_011528209.2:c.887-1G=	XP_011526511.1:n.887-1G=
XR_001753738.2:n.1919G=
XR_001753740.2:n.1889G=
NM_000455.5:c.1113G= MANE Select	NP_000446.1:p.Gln371=