Canonical Allele Identifier: CA2317590339

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1221269T= , CM000681.2:g.1221269T=	GRCh38
NC_000019.9:g.1221268T= , CM000681.1:g.1221268T=	GRCh37
NC_000019.8:g.1172268T=	NCBI36
NG_007460.2:g.36863T= , LRG_319:g.36863T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.791T=	ENSP00000490268.2:p.Phe264=
ENST00000585748.3:c.419T=	ENSP00000477641.2:p.Phe140=
ENST00000585851.2:c.617T=	ENSP00000467912.2:p.Phe206=
ENST00000326873.12:c.791T= MANE Select	ENSP00000324856.6:p.Phe264=
ENST00000652231.1:c.791T=	ENSP00000498804.1:p.Phe264=
ENST00000326873.11:c.791T=	ENSP00000324856.6:p.Phe264=
ENST00000586243.5:c.791T=	ENSP00000467240.2:p.Phe264=
ENST00000586358.5:n.689T=
ENST00000589152.5:n.881T=
ENST00000591133.2:n.762T=
NM_000455.4:c.791T= , LRG_319t1:c.791T=	NP_000446.1:p.Phe264=
XM_005259617.1:c.791T=	XP_005259674.1:p.Phe264=
XM_005259618.3:c.791T=	XP_005259675.1:p.Phe264=
XM_011528209.1:c.569T=	XP_011526511.1:p.Phe190=
XR_936204.1:n.1416T=
XM_005259617.3:c.791T=	XP_005259674.1:p.Phe264=
XM_011528209.2:c.569T=	XP_011526511.1:p.Phe190=
XR_001753738.2:n.1416T=
XR_001753739.1:n.1416T=
XR_001753740.2:n.1416T=
NM_000455.5:c.791T= MANE Select	NP_000446.1:p.Phe264=