Canonical Allele Identifier: CA2317593499

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226237C= , CM000681.2:g.1226237C=	GRCh38
NC_000019.9:g.1226236C= , CM000681.1:g.1226236C=	GRCh37
NC_000019.8:g.1177236C=	NCBI36
NG_007460.2:g.41831C= , LRG_319:g.41831C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2493C=	ENSP00000490268.2:n.*2493C=
ENST00000585748.3:c.737-217C=	ENSP00000477641.2:n.737-217C=
ENST00000585851.2:c.935-217C=	ENSP00000467912.2:n.935-217C=
ENST00000326873.12:c.1109-217C= MANE Select	ENSP00000324856.6:n.1109-217C=
ENST00000326873.11:c.1109-217C=	ENSP00000324856.6:n.1109-217C=
ENST00000585465.2:n.2625C=
ENST00000586243.5:c.1109-217C=	ENSP00000467240.2:n.1109-217C=
ENST00000589152.5:n.1807-217C=
NM_000455.4:c.1109-217C= , LRG_319t1:c.1109-217C=	NP_000446.1:n.1109-217C=
XM_005259617.1:c.1109-222C=	XP_005259674.1:n.1109-222C=
XM_011528209.1:c.887-222C=	XP_011526511.1:n.887-222C=
XM_005259617.3:c.1109-222C=	XP_005259674.1:n.1109-222C=
XM_011528209.2:c.887-222C=	XP_011526511.1:n.887-222C=
XR_001753738.2:n.1915-217C=
XR_001753740.2:n.1885-217C=
NM_000455.5:c.1109-217C= MANE Select	NP_000446.1:n.1109-217C=