Canonical Allele Identifier: CA2317590041

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220810G= , CM000681.2:g.1220810G=	GRCh38
NC_000019.9:g.1220809G= , CM000681.1:g.1220809G=	GRCh37
NC_000019.8:g.1171809G=	NCBI36
NG_007460.2:g.36404G= , LRG_319:g.36404G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.734+93G=	ENSP00000490268.2:n.734+93G=
ENST00000585748.3:c.362+93G=	ENSP00000477641.2:n.362+93G=
ENST00000585851.2:c.560+93G=	ENSP00000467912.2:n.560+93G=
ENST00000326873.12:c.734+93G= MANE Select	ENSP00000324856.6:n.734+93G=
ENST00000652231.1:c.734+93G=	ENSP00000498804.1:n.734+93G=
ENST00000326873.11:c.734+93G=	ENSP00000324856.6:n.734+93G=
ENST00000586243.5:c.734+93G=	ENSP00000467240.2:n.734+93G=
ENST00000586358.5:n.632+93G=
ENST00000589152.5:n.824+93G=
ENST00000591133.2:n.705+93G=
NM_000455.4:c.734+93G= , LRG_319t1:c.734+93G=	NP_000446.1:n.734+93G=
XM_005259617.1:c.734+93G=	XP_005259674.1:n.734+93G=
XM_005259618.3:c.734+93G=	XP_005259675.1:n.734+93G=
XM_011528209.1:c.512+93G=	XP_011526511.1:n.512+93G=
XR_936204.1:n.1359+93G=
XM_005259617.3:c.734+93G=	XP_005259674.1:n.734+93G=
XM_011528209.2:c.512+93G=	XP_011526511.1:n.512+93G=
XR_001753738.2:n.1359+93G=
XR_001753739.1:n.1359+93G=
XR_001753740.2:n.1359+93G=
NM_000455.5:c.734+93G= MANE Select	NP_000446.1:n.734+93G=