Canonical Allele Identifier: CA2317593767

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226597T= , CM000681.2:g.1226597T=	GRCh38
NC_000019.9:g.1226596T= , CM000681.1:g.1226596T=	GRCh37
NC_000019.8:g.1177596T=	NCBI36
NG_007460.2:g.42191T= , LRG_319:g.42191T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000455.5:c.1252T= MANE Select	NP_000446.1:p.Cys418=
ENST00000326873.12:c.1252T= MANE Select	ENSP00000324856.6:p.Cys418=
NM_000455.4:c.1252T= , LRG_319t1:c.1252T=	NP_000446.1:p.Cys418=
ENST00000326873.11:c.1252T=	ENSP00000324856.6:p.Cys418=
ENST00000585465.2:n.2985T=
ENST00000585465.3:c.*2853T=	ENSP00000490268.2:n.*2853T=
ENST00000585748.3:c.880T=	ENSP00000477641.2:p.Cys294=
ENST00000585851.2:c.1078T=	ENSP00000467912.2:p.Cys360=
ENST00000586243.5:c.1251T=	ENSP00000467240.2:p.Pro417=
ENST00000589152.5:n.1950T=
XM_005259617.1:c.1247T=	XP_005259674.1:p.Leu416=
XM_005259617.3:c.1247T=	XP_005259674.1:p.Leu416=
XM_011528209.1:c.1025T=	XP_011526511.1:p.Leu342=
XM_011528209.2:c.1025T=	XP_011526511.1:p.Leu342=
XR_001753738.2:n.2058T=
XR_001753740.2:n.2028T=