Canonical Allele Identifier: CA2317581539
Gene: STK11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1206924T= , CM000681.2:g.1206924T= GRCh38
NC_000019.9:g.1206923T= , CM000681.1:g.1206923T= GRCh37
NC_000019.8:g.1157923T= NCBI36
NG_007460.2:g.22518T= , LRG_319:g.22518T=

Transcript Alleles

HGVS Amino-acid change
ENST00000585465.3:c.11T= ENSP00000490268.2:p.Val4=
ENST00000585748.3:c.-82-11493T= ENSP00000477641.2:n.-82-11493T=
ENST00000585851.2:c.11T= ENSP00000467912.2:p.Val4=
ENST00000326873.12:c.11T= MANE Select ENSP00000324856.6:p.Val4=
ENST00000652231.1:c.11T= ENSP00000498804.1:p.Val4=
ENST00000326873.11:c.11T= ENSP00000324856.6:p.Val4=
ENST00000585748.2:c.-82-11493T= ENSP00000477641.1:n.-82-11493T=
ENST00000585851.1:c.11T= ENSP00000467912.1:p.Val4=
ENST00000586243.5:c.11T= ENSP00000467240.2:p.Val4=
ENST00000589152.5:n.101T=
ENST00000593219.5:c.11T= ENSP00000466610.1:p.Val4=
NM_000455.4:c.11T= , LRG_319t1:c.11T= NP_000446.1:p.Val4=
XM_005259617.1:c.11T= XP_005259674.1:p.Val4=
XM_005259618.3:c.11T= XP_005259675.1:p.Val4=
XM_011528209.1:c.-343T= XP_011526511.1:n.-343T=
XR_936204.1:n.636T=
XM_005259617.3:c.11T= XP_005259674.1:p.Val4=
XM_011528209.2:c.-343T= XP_011526511.1:n.-343T=
XR_001753738.2:n.636T=
XR_001753739.1:n.636T=
XR_001753740.2:n.636T=
NM_000455.5:c.11T= MANE Select NP_000446.1:p.Val4=