Canonical Allele Identifier: CA402953176

Gene: STK11

Linked Data

• MyVariant Identifiers: chr19:g.1226465A>T (hg19) ; chr19:g.1226466A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226466A>T , CM000681.2:g.1226466A>T	GRCh38
NC_000019.9:g.1226465A>T , CM000681.1:g.1226465A>T	GRCh37
NC_000019.8:g.1177465A>T	NCBI36
NG_007460.2:g.42060A>T , LRG_319:g.42060A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2722A>T	ENSP00000490268.2:n.*2722A>T
ENST00000585748.3:c.749A>T	ENSP00000477641.2:p.Glu250Val
ENST00000585851.2:c.947A>T	ENSP00000467912.2:p.Glu316Val
ENST00000326873.12:c.1121A>T MANE Select	ENSP00000324856.6:p.Glu374Val
ENST00000326873.11:c.1121A>T	ENSP00000324856.6:p.Glu374Val
ENST00000585465.2:n.2854A>T
ENST00000586243.5:c.1121A>T	ENSP00000467240.2:p.Glu374Val
ENST00000589152.5:n.1819A>T
NM_000455.4:c.1121A>T , LRG_319t1:c.1121A>T	NP_000446.1:p.Glu374Val
XM_005259617.1:c.1116A>T	XP_005259674.1:p.Arg372Ser
XM_011528209.1:c.894A>T	XP_011526511.1:p.Arg298Ser
XM_005259617.3:c.1116A>T	XP_005259674.1:p.Arg372Ser
XM_011528209.2:c.894A>T	XP_011526511.1:p.Arg298Ser
XR_001753738.2:n.1927A>T
XR_001753740.2:n.1897A>T
NM_000455.5:c.1121A>T MANE Select	NP_000446.1:p.Glu374Val