Canonical Allele Identifier: CA2317593786

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226612A= , CM000681.2:g.1226612A=	GRCh38
NC_000019.9:g.1226611A= , CM000681.1:g.1226611A=	GRCh37
NC_000019.8:g.1177611A=	NCBI36
NG_007460.2:g.42206A= , LRG_319:g.42206A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2868A=	ENSP00000490268.2:n.*2868A=
ENST00000585748.3:c.895A=	ENSP00000477641.2:p.Lys299=
ENST00000585851.2:c.1093A=	ENSP00000467912.2:p.Lys365=
ENST00000326873.12:c.1267A= MANE Select	ENSP00000324856.6:p.Lys423=
ENST00000326873.11:c.1267A=	ENSP00000324856.6:p.Lys423=
ENST00000585465.2:n.3000A=
ENST00000586243.5:c.1264A=	ENSP00000467240.2:p.Lys422=
ENST00000589152.5:n.1965A=
NM_000455.4:c.1267A= , LRG_319t1:c.1267A=	NP_000446.1:p.Lys423=
XM_005259617.1:c.1262A=	XP_005259674.1:p.Gln421=
XM_011528209.1:c.1040A=	XP_011526511.1:p.Gln347=
XM_005259617.3:c.1262A=	XP_005259674.1:p.Gln421=
XM_011528209.2:c.1040A=	XP_011526511.1:p.Gln347=
XR_001753738.2:n.2073A=
XR_001753740.2:n.2043A=
NM_000455.5:c.1267A= MANE Select	NP_000446.1:p.Lys423=