Canonical Allele Identifier: CA2317593702

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226523A= , CM000681.2:g.1226523A=	GRCh38
NC_000019.9:g.1226522A= , CM000681.1:g.1226522A=	GRCh37
NC_000019.8:g.1177522A=	NCBI36
NG_007460.2:g.42117A= , LRG_319:g.42117A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2779A=	ENSP00000490268.2:n.*2779A=
ENST00000585748.3:c.806A=	ENSP00000477641.2:p.Asn269=
ENST00000585851.2:c.1004A=	ENSP00000467912.2:p.Asn335=
ENST00000326873.12:c.1178A= MANE Select	ENSP00000324856.6:p.Asn393=
ENST00000326873.11:c.1178A=	ENSP00000324856.6:p.Asn393=
ENST00000585465.2:n.2911A=
ENST00000586243.5:c.1178A=	ENSP00000467240.2:p.Asn393=
ENST00000589152.5:n.1876A=
NM_000455.4:c.1178A= , LRG_319t1:c.1178A=	NP_000446.1:p.Asn393=
XM_005259617.1:c.1173A=	XP_005259674.1:p.Glu391=
XM_011528209.1:c.951A=	XP_011526511.1:p.Glu317=
XM_005259617.3:c.1173A=	XP_005259674.1:p.Glu391=
XM_011528209.2:c.951A=	XP_011526511.1:p.Glu317=
XR_001753738.2:n.1984A=
XR_001753740.2:n.1954A=
NM_000455.5:c.1178A= MANE Select	NP_000446.1:p.Asn393=