Canonical Allele Identifier: CA2317593753

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226580A= , CM000681.2:g.1226580A=	GRCh38
NC_000019.9:g.1226579A= , CM000681.1:g.1226579A=	GRCh37
NC_000019.8:g.1177579A=	NCBI36
NG_007460.2:g.42174A= , LRG_319:g.42174A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2836A=	ENSP00000490268.2:n.*2836A=
ENST00000585748.3:c.863A=	ENSP00000477641.2:p.Asn288=
ENST00000585851.2:c.1061A=	ENSP00000467912.2:p.Asn354=
ENST00000326873.12:c.1235A= MANE Select	ENSP00000324856.6:p.Asn412=
ENST00000326873.11:c.1235A=	ENSP00000324856.6:p.Asn412=
ENST00000585465.2:n.2968A=
ENST00000586243.5:c.1234A=	ENSP00000467240.2:p.Thr412=
ENST00000589152.5:n.1933A=
NM_000455.4:c.1235A= , LRG_319t1:c.1235A=	NP_000446.1:p.Asn412=
XM_005259617.1:c.1230A=	XP_005259674.1:p.Gln410=
XM_011528209.1:c.1008A=	XP_011526511.1:p.Gln336=
XM_005259617.3:c.1230A=	XP_005259674.1:p.Gln410=
XM_011528209.2:c.1008A=	XP_011526511.1:p.Gln336=
XR_001753738.2:n.2041A=
XR_001753740.2:n.2011A=
NM_000455.5:c.1235A= MANE Select	NP_000446.1:p.Asn412=