Canonical Allele Identifier: CA2317593684

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226499G= , CM000681.2:g.1226499G=	GRCh38
NC_000019.9:g.1226498G= , CM000681.1:g.1226498G=	GRCh37
NC_000019.8:g.1177498G=	NCBI36
NG_007460.2:g.42093G= , LRG_319:g.42093G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000455.5:c.1154G= MANE Select	NP_000446.1:p.Gly385=
ENST00000326873.12:c.1154G= MANE Select	ENSP00000324856.6:p.Gly385=
NM_000455.4:c.1154G= , LRG_319t1:c.1154G=	NP_000446.1:p.Gly385=
ENST00000326873.11:c.1154G=	ENSP00000324856.6:p.Gly385=
ENST00000585465.2:n.2887G=
ENST00000585465.3:c.*2755G=	ENSP00000490268.2:n.*2755G=
ENST00000585748.3:c.782G=	ENSP00000477641.2:p.Gly261=
ENST00000585851.2:c.980G=	ENSP00000467912.2:p.Gly327=
ENST00000586243.5:c.1154G=	ENSP00000467240.2:p.Gly385=
ENST00000589152.5:n.1852G=
XM_005259617.1:c.1149G=	XP_005259674.1:p.Gly383=
XM_005259617.3:c.1149G=	XP_005259674.1:p.Gly383=
XM_011528209.1:c.927G=	XP_011526511.1:p.Gly309=
XM_011528209.2:c.927G=	XP_011526511.1:p.Gly309=
XR_001753738.2:n.1960G=
XR_001753740.2:n.1930G=