Canonical Allele Identifier: CA2317591562

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1223136G= , CM000681.2:g.1223136G=	GRCh38
NC_000019.9:g.1223135G= , CM000681.1:g.1223135G=	GRCh37
NC_000019.8:g.1174135G=	NCBI36
NG_007460.2:g.38730G= , LRG_319:g.38730G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.1072G=	ENSP00000490268.2:p.Asp358=
ENST00000585748.3:c.700G=	ENSP00000477641.2:p.Asp234=
ENST00000585851.2:c.898G=	ENSP00000467912.2:p.Asp300=
ENST00000326873.12:c.1072G= MANE Select	ENSP00000324856.6:p.Asp358=
ENST00000652231.1:c.1072G=	ENSP00000498804.1:p.Asp358=
ENST00000326873.11:c.1072G=	ENSP00000324856.6:p.Asp358=
ENST00000586243.5:c.1072G=	ENSP00000467240.2:p.Asp358=
ENST00000589152.5:n.1770G=
NM_000455.4:c.1072G= , LRG_319t1:c.1072G=	NP_000446.1:p.Asp358=
XM_005259617.1:c.1072G=	XP_005259674.1:p.Asp358=
XM_005259618.3:c.1072G=	XP_005259675.1:p.Asp358=
XM_011528209.1:c.850G=	XP_011526511.1:p.Asp284=
XR_936204.1:n.1848G=
XM_005259617.3:c.1072G=	XP_005259674.1:p.Asp358=
XM_011528209.2:c.850G=	XP_011526511.1:p.Asp284=
XR_001753738.2:n.1878G=
XR_001753739.1:n.1878G=
XR_001753740.2:n.1848G=
NM_000455.5:c.1072G= MANE Select	NP_000446.1:p.Asp358=