Canonical Allele Identifier: CA2317593698

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226518T= , CM000681.2:g.1226518T=	GRCh38
NC_000019.9:g.1226517T= , CM000681.1:g.1226517T=	GRCh37
NC_000019.8:g.1177517T=	NCBI36
NG_007460.2:g.42112T= , LRG_319:g.42112T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2774T=	ENSP00000490268.2:n.*2774T=
ENST00000585748.3:c.801T=	ENSP00000477641.2:p.Cys267=
ENST00000585851.2:c.999T=	ENSP00000467912.2:p.Cys333=
ENST00000326873.12:c.1173T= MANE Select	ENSP00000324856.6:p.Cys391=
ENST00000326873.11:c.1173T=	ENSP00000324856.6:p.Cys391=
ENST00000585465.2:n.2906T=
ENST00000586243.5:c.1173T=	ENSP00000467240.2:p.Cys391=
ENST00000589152.5:n.1871T=
NM_000455.4:c.1173T= , LRG_319t1:c.1173T=	NP_000446.1:p.Cys391=
XM_005259617.1:c.1168T=	XP_005259674.1:p.Tyr390=
XM_011528209.1:c.946T=	XP_011526511.1:p.Tyr316=
XM_005259617.3:c.1168T=	XP_005259674.1:p.Tyr390=
XM_011528209.2:c.946T=	XP_011526511.1:p.Tyr316=
XR_001753738.2:n.1979T=
XR_001753740.2:n.1949T=
NM_000455.5:c.1173T= MANE Select	NP_000446.1:p.Cys391=