Canonical Allele Identifier: CA645604057
Gene: STK11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1218406_1218431del , CM000681.2:g.1218406_1218431del GRCh38
NC_000019.9:g.1218405_1218430del , CM000681.1:g.1218405_1218430del GRCh37
NC_000019.8:g.1169405_1169430del NCBI36
NG_007460.2:g.34000_34025del , LRG_319:g.34000_34025del

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.291-11_305del
ENST00000585748.3:c.-82-11_-68del
ENST00000585851.2:c.291-1967_291-1942del ENSP00000467912.2:n.291-1967_291-1942del
ENST00000326873.12:c.291-11_305del
ENST00000652231.1:c.291-11_305del
ENST00000326873.11:c.291-11_305del
ENST00000585748.2:c.-82-11_-68del
ENST00000585851.1:c.291-1967_291-1942del ENSP00000467912.1:n.291-1967_291-1942del
ENST00000586243.5:c.291-11_305del
ENST00000586358.5:n.114-11_128del
ENST00000589152.5:n.381-11_395del
ENST00000593219.5:c.*116-11_*130del
NM_000455.4:c.291-11_305del , LRG_319t1:c.291-11_305del
XM_005259617.1:c.291-11_305del
XM_005259618.3:c.291-11_305del
XM_011528209.1:c.69-11_83del
XR_936204.1:n.916-11_930del
XM_005259617.3:c.291-11_305del
XM_011528209.2:c.69-11_83del
XR_001753738.2:n.916-11_930del
XR_001753739.1:n.916-11_930del
XR_001753740.2:n.916-11_930del
NM_000455.5:c.291-11_305del