Canonical Allele Identifier: CA2317581496

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1206866C= , CM000681.2:g.1206866C=	GRCh38
NC_000019.9:g.1206865C= , CM000681.1:g.1206865C=	GRCh37
NC_000019.8:g.1157865C=	NCBI36
NG_007460.2:g.22460C= , LRG_319:g.22460C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.-48C=	ENSP00000490268.2:n.-48C=
ENST00000585748.3:c.-82-11551C=	ENSP00000477641.2:n.-82-11551C=
ENST00000326873.12:c.-48C= MANE Select	ENSP00000324856.6:n.-48C=
ENST00000652231.1:c.-48C=	ENSP00000498804.1:n.-48C=
ENST00000326873.11:c.-48C=	ENSP00000324856.6:n.-48C=
ENST00000585748.2:c.-82-11551C=	ENSP00000477641.1:n.-82-11551C=
ENST00000586243.5:c.-48C=	ENSP00000467240.2:n.-48C=
ENST00000589152.5:n.43C=
ENST00000593219.5:c.-48C=	ENSP00000466610.1:n.-48C=
NM_000455.4:c.-48C= , LRG_319t1:c.-48C=	NP_000446.1:n.-48C=
XM_005259617.1:c.-48C=	XP_005259674.1:n.-48C=
XM_005259618.3:c.-48C=	XP_005259675.1:n.-48C=
XM_011528209.1:c.-401C=	XP_011526511.1:n.-401C=
XR_936204.1:n.578C=
XM_005259617.3:c.-48C=	XP_005259674.1:n.-48C=
XM_011528209.2:c.-401C=	XP_011526511.1:n.-401C=
XR_001753738.2:n.578C=
XR_001753739.1:n.578C=
XR_001753740.2:n.578C=
NM_000455.5:c.-48C= MANE Select	NP_000446.1:n.-48C=