Canonical Allele Identifier: CA2317593759

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226588C= , CM000681.2:g.1226588C=	GRCh38
NC_000019.9:g.1226587C= , CM000681.1:g.1226587C=	GRCh37
NC_000019.8:g.1177587C=	NCBI36
NG_007460.2:g.42182C= , LRG_319:g.42182C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2844C=	ENSP00000490268.2:n.*2844C=
ENST00000585748.3:c.871C=	ENSP00000477641.2:p.Arg291=
ENST00000585851.2:c.1069C=	ENSP00000467912.2:p.Arg357=
ENST00000326873.12:c.1243C= MANE Select	ENSP00000324856.6:p.Arg415=
ENST00000326873.11:c.1243C=	ENSP00000324856.6:p.Arg415=
ENST00000585465.2:n.2976C=
ENST00000586243.5:c.1242C=	ENSP00000467240.2:p.Pro414=
ENST00000589152.5:n.1941C=
NM_000455.4:c.1243C= , LRG_319t1:c.1243C=	NP_000446.1:p.Arg415=
XM_005259617.1:c.1238C=	XP_005259674.1:p.Pro413=
XM_011528209.1:c.1016C=	XP_011526511.1:p.Pro339=
XM_005259617.3:c.1238C=	XP_005259674.1:p.Pro413=
XM_011528209.2:c.1016C=	XP_011526511.1:p.Pro339=
XR_001753738.2:n.2049C=
XR_001753740.2:n.2019C=
NM_000455.5:c.1243C= MANE Select	NP_000446.1:p.Arg415=