Canonical Allele Identifier: CA2317593756

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226583C= , CM000681.2:g.1226583C=	GRCh38
NC_000019.9:g.1226582C= , CM000681.1:g.1226582C=	GRCh37
NC_000019.8:g.1177582C=	NCBI36
NG_007460.2:g.42177C= , LRG_319:g.42177C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2839C=	ENSP00000490268.2:n.*2839C=
ENST00000585748.3:c.866C=	ENSP00000477641.2:p.Pro289=
ENST00000585851.2:c.1064C=	ENSP00000467912.2:p.Pro355=
ENST00000326873.12:c.1238C= MANE Select	ENSP00000324856.6:p.Pro413=
ENST00000326873.11:c.1238C=	ENSP00000324856.6:p.Pro413=
ENST00000585465.2:n.2971C=
ENST00000586243.5:c.1237C=	ENSP00000467240.2:p.Leu413=
ENST00000589152.5:n.1936C=
NM_000455.4:c.1238C= , LRG_319t1:c.1238C=	NP_000446.1:p.Pro413=
XM_005259617.1:c.1233C=	XP_005259674.1:p.Pro411=
XM_011528209.1:c.1011C=	XP_011526511.1:p.Pro337=
XM_005259617.3:c.1233C=	XP_005259674.1:p.Pro411=
XM_011528209.2:c.1011C=	XP_011526511.1:p.Pro337=
XR_001753738.2:n.2044C=
XR_001753740.2:n.2014C=
NM_000455.5:c.1238C= MANE Select	NP_000446.1:p.Pro413=