Canonical Allele Identifier: CA402948154

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219343T>C , CM000681.2:g.1219343T>C	GRCh38
NC_000019.9:g.1219342T>C , CM000681.1:g.1219342T>C	GRCh37
NC_000019.8:g.1170342T>C	NCBI36
NG_007460.2:g.34937T>C , LRG_319:g.34937T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000455.5:c.394T>C MANE Select	NP_000446.1:p.Cys132Arg
ENST00000326873.12:c.394T>C MANE Select	ENSP00000324856.6:p.Cys132Arg
NM_000455.4:c.394T>C , LRG_319t1:c.394T>C	NP_000446.1:p.Cys132Arg
ENST00000326873.11:c.394T>C	ENSP00000324856.6:p.Cys132Arg
ENST00000585465.3:c.394T>C	ENSP00000490268.2:p.Cys132Arg
ENST00000585748.2:c.22T>C	ENSP00000477641.1:p.Cys8Arg
ENST00000585748.3:c.22T>C	ENSP00000477641.2:p.Cys8Arg
ENST00000585851.1:c.291-1030T>C	ENSP00000467912.1:n.291-1030T>C
ENST00000585851.2:c.291-1030T>C	ENSP00000467912.2:n.291-1030T>C
ENST00000586243.5:c.394T>C	ENSP00000467240.2:p.Cys132Arg
ENST00000586358.5:n.217T>C
ENST00000589152.5:n.484T>C
ENST00000593219.5:c.*219T>C	ENSP00000466610.1:n.*219T>C
ENST00000652231.1:c.394T>C	ENSP00000498804.1:p.Cys132Arg
XM_005259617.1:c.394T>C	XP_005259674.1:p.Cys132Arg
XM_005259617.3:c.394T>C	XP_005259674.1:p.Cys132Arg
XM_005259618.3:c.394T>C	XP_005259675.1:p.Cys132Arg
XM_011528209.1:c.172T>C	XP_011526511.1:p.Cys58Arg
XM_011528209.2:c.172T>C	XP_011526511.1:p.Cys58Arg
XR_001753738.2:n.1019T>C
XR_001753739.1:n.1019T>C
XR_001753740.2:n.1019T>C
XR_936204.1:n.1019T>C