Canonical Allele Identifier: CA2317588556

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218481A= , CM000681.2:g.1218481A=	GRCh38
NC_000019.9:g.1218480A= , CM000681.1:g.1218480A=	GRCh37
NC_000019.8:g.1169480A=	NCBI36
NG_007460.2:g.34075A= , LRG_319:g.34075A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.355A=	ENSP00000490268.2:p.Asn119=
ENST00000585748.3:c.-18A=	ENSP00000477641.2:n.-18A=
ENST00000585851.2:c.291-1892A=	ENSP00000467912.2:n.291-1892A=
ENST00000326873.12:c.355A= MANE Select	ENSP00000324856.6:p.Asn119=
ENST00000652231.1:c.355A=	ENSP00000498804.1:p.Asn119=
ENST00000326873.11:c.355A=	ENSP00000324856.6:p.Asn119=
ENST00000585748.2:c.-18A=	ENSP00000477641.1:n.-18A=
ENST00000585851.1:c.291-1892A=	ENSP00000467912.1:n.291-1892A=
ENST00000586243.5:c.355A=	ENSP00000467240.2:p.Asn119=
ENST00000586358.5:n.178A=
ENST00000589152.5:n.445A=
ENST00000593219.5:c.*180A=	ENSP00000466610.1:n.*180A=
NM_000455.4:c.355A= , LRG_319t1:c.355A=	NP_000446.1:p.Asn119=
XM_005259617.1:c.355A=	XP_005259674.1:p.Asn119=
XM_005259618.3:c.355A=	XP_005259675.1:p.Asn119=
XM_011528209.1:c.133A=	XP_011526511.1:p.Asn45=
XR_936204.1:n.980A=
XM_005259617.3:c.355A=	XP_005259674.1:p.Asn119=
XM_011528209.2:c.133A=	XP_011526511.1:p.Asn45=
XR_001753738.2:n.980A=
XR_001753739.1:n.980A=
XR_001753740.2:n.980A=
NM_000455.5:c.355A= MANE Select	NP_000446.1:p.Asn119=