Canonical Allele Identifier: CA2317590269

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1221172C= , CM000681.2:g.1221172C=	GRCh38
NC_000019.9:g.1221171C= , CM000681.1:g.1221171C=	GRCh37
NC_000019.8:g.1172171C=	NCBI36
NG_007460.2:g.36766C= , LRG_319:g.36766C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.735-41C=	ENSP00000490268.2:n.735-41C=
ENST00000585748.3:c.363-41C=	ENSP00000477641.2:n.363-41C=
ENST00000585851.2:c.561-41C=	ENSP00000467912.2:n.561-41C=
ENST00000326873.12:c.735-41C= MANE Select	ENSP00000324856.6:n.735-41C=
ENST00000652231.1:c.735-41C=	ENSP00000498804.1:n.735-41C=
ENST00000326873.11:c.735-41C=	ENSP00000324856.6:n.735-41C=
ENST00000586243.5:c.735-41C=	ENSP00000467240.2:n.735-41C=
ENST00000586358.5:n.633-41C=
ENST00000589152.5:n.825-41C=
ENST00000591133.2:n.706-41C=
NM_000455.4:c.735-41C= , LRG_319t1:c.735-41C=	NP_000446.1:n.735-41C=
XM_005259617.1:c.735-41C=	XP_005259674.1:n.735-41C=
XM_005259618.3:c.735-41C=	XP_005259675.1:n.735-41C=
XM_011528209.1:c.513-41C=	XP_011526511.1:n.513-41C=
XR_936204.1:n.1360-41C=
XM_005259617.3:c.735-41C=	XP_005259674.1:n.735-41C=
XM_011528209.2:c.513-41C=	XP_011526511.1:n.513-41C=
XR_001753738.2:n.1360-41C=
XR_001753739.1:n.1360-41C=
XR_001753740.2:n.1360-41C=
NM_000455.5:c.735-41C= MANE Select	NP_000446.1:n.735-41C=