Canonical Allele Identifier: CA2317588558

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218483C= , CM000681.2:g.1218483C=	GRCh38
NC_000019.9:g.1218482C= , CM000681.1:g.1218482C=	GRCh37
NC_000019.8:g.1169482C=	NCBI36
NG_007460.2:g.34077C= , LRG_319:g.34077C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.357C=	ENSP00000490268.2:p.Asn119=
ENST00000585748.3:c.-16C=	ENSP00000477641.2:n.-16C=
ENST00000585851.2:c.291-1890C=	ENSP00000467912.2:n.291-1890C=
ENST00000326873.12:c.357C= MANE Select	ENSP00000324856.6:p.Asn119=
ENST00000652231.1:c.357C=	ENSP00000498804.1:p.Asn119=
ENST00000326873.11:c.357C=	ENSP00000324856.6:p.Asn119=
ENST00000585748.2:c.-16C=	ENSP00000477641.1:n.-16C=
ENST00000585851.1:c.291-1890C=	ENSP00000467912.1:n.291-1890C=
ENST00000586243.5:c.357C=	ENSP00000467240.2:p.Asn119=
ENST00000586358.5:n.180C=
ENST00000589152.5:n.447C=
ENST00000593219.5:c.*182C=	ENSP00000466610.1:n.*182C=
NM_000455.4:c.357C= , LRG_319t1:c.357C=	NP_000446.1:p.Asn119=
XM_005259617.1:c.357C=	XP_005259674.1:p.Asn119=
XM_005259618.3:c.357C=	XP_005259675.1:p.Asn119=
XM_011528209.1:c.135C=	XP_011526511.1:p.Asn45=
XR_936204.1:n.982C=
XM_005259617.3:c.357C=	XP_005259674.1:p.Asn119=
XM_011528209.2:c.135C=	XP_011526511.1:p.Asn45=
XR_001753738.2:n.982C=
XR_001753739.1:n.982C=
XR_001753740.2:n.982C=
NM_000455.5:c.357C= MANE Select	NP_000446.1:p.Asn119=