Canonical Allele Identifier: CA2317591473

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1223027C= , CM000681.2:g.1223027C=	GRCh38
NC_000019.9:g.1223026C= , CM000681.1:g.1223026C=	GRCh37
NC_000019.8:g.1174026C=	NCBI36
NG_007460.2:g.38621C= , LRG_319:g.38621C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.963C=	ENSP00000490268.2:p.Pro321=
ENST00000585748.3:c.591C=	ENSP00000477641.2:p.Pro197=
ENST00000585851.2:c.789C=	ENSP00000467912.2:p.Pro263=
ENST00000326873.12:c.963C= MANE Select	ENSP00000324856.6:p.Pro321=
ENST00000652231.1:c.963C=	ENSP00000498804.1:p.Pro321=
ENST00000326873.11:c.963C=	ENSP00000324856.6:p.Pro321=
ENST00000586243.5:c.963C=	ENSP00000467240.2:p.Pro321=
ENST00000589152.5:n.1661C=
ENST00000591133.2:n.934C=
NM_000455.4:c.963C= , LRG_319t1:c.963C=	NP_000446.1:p.Pro321=
XM_005259617.1:c.963C=	XP_005259674.1:p.Pro321=
XM_005259618.3:c.963C=	XP_005259675.1:p.Pro321=
XM_011528209.1:c.741C=	XP_011526511.1:p.Pro247=
XR_936204.1:n.1739C=
XM_005259617.3:c.963C=	XP_005259674.1:p.Pro321=
XM_011528209.2:c.741C=	XP_011526511.1:p.Pro247=
XR_001753738.2:n.1769C=
XR_001753739.1:n.1769C=
XR_001753740.2:n.1739C=
NM_000455.5:c.963C= MANE Select	NP_000446.1:p.Pro321=