Canonical Allele Identifier: CA2317593528

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226276G= , CM000681.2:g.1226276G=	GRCh38
NC_000019.9:g.1226275G= , CM000681.1:g.1226275G=	GRCh37
NC_000019.8:g.1177275G=	NCBI36
NG_007460.2:g.41870G= , LRG_319:g.41870G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2532G=	ENSP00000490268.2:n.*2532G=
ENST00000585748.3:c.737-178G=	ENSP00000477641.2:n.737-178G=
ENST00000585851.2:c.935-178G=	ENSP00000467912.2:n.935-178G=
ENST00000326873.12:c.1109-178G= MANE Select	ENSP00000324856.6:n.1109-178G=
ENST00000326873.11:c.1109-178G=	ENSP00000324856.6:n.1109-178G=
ENST00000585465.2:n.2664G=
ENST00000586243.5:c.1109-178G=	ENSP00000467240.2:n.1109-178G=
ENST00000589152.5:n.1807-178G=
NM_000455.4:c.1109-178G= , LRG_319t1:c.1109-178G=	NP_000446.1:n.1109-178G=
XM_005259617.1:c.1109-183G=	XP_005259674.1:n.1109-183G=
XM_011528209.1:c.887-183G=	XP_011526511.1:n.887-183G=
XM_005259617.3:c.1109-183G=	XP_005259674.1:n.1109-183G=
XM_011528209.2:c.887-183G=	XP_011526511.1:n.887-183G=
XR_001753738.2:n.1915-178G=
XR_001753740.2:n.1885-178G=
NM_000455.5:c.1109-178G= MANE Select	NP_000446.1:n.1109-178G=