Canonical Allele Identifier: CA2317593510

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226250C= , CM000681.2:g.1226250C=	GRCh38
NC_000019.9:g.1226249C= , CM000681.1:g.1226249C=	GRCh37
NC_000019.8:g.1177249C=	NCBI36
NG_007460.2:g.41844C= , LRG_319:g.41844C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2506C=	ENSP00000490268.2:n.*2506C=
ENST00000585748.3:c.737-204C=	ENSP00000477641.2:n.737-204C=
ENST00000585851.2:c.935-204C=	ENSP00000467912.2:n.935-204C=
ENST00000326873.12:c.1109-204C= MANE Select	ENSP00000324856.6:n.1109-204C=
ENST00000326873.11:c.1109-204C=	ENSP00000324856.6:n.1109-204C=
ENST00000585465.2:n.2638C=
ENST00000586243.5:c.1109-204C=	ENSP00000467240.2:n.1109-204C=
ENST00000589152.5:n.1807-204C=
NM_000455.4:c.1109-204C= , LRG_319t1:c.1109-204C=	NP_000446.1:n.1109-204C=
XM_005259617.1:c.1109-209C=	XP_005259674.1:n.1109-209C=
XM_011528209.1:c.887-209C=	XP_011526511.1:n.887-209C=
XM_005259617.3:c.1109-209C=	XP_005259674.1:n.1109-209C=
XM_011528209.2:c.887-209C=	XP_011526511.1:n.887-209C=
XR_001753738.2:n.1915-204C=
XR_001753740.2:n.1885-204C=
NM_000455.5:c.1109-204C= MANE Select	NP_000446.1:n.1109-204C=