Canonical Allele Identifier: CA3265808143

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218321_1218443del , CM000681.2:g.1218321_1218443del	GRCh38
NC_000019.9:g.1218320_1218442del , CM000681.1:g.1218320_1218442del	GRCh37
NC_000019.8:g.1169320_1169442del	NCBI36
NG_007460.2:g.33915_34037del , LRG_319:g.33915_34037del

Transcript Alleles

HGVS	Amino-acid Change
NM_000455.4:c.291-96_317del , LRG_319t1:c.291-96_317del
NM_000455.5:c.291-96_317del
ENST00000326873.11:c.291-96_317del
ENST00000326873.12:c.291-96_317del
ENST00000585465.3:c.291-96_317del
ENST00000585748.2:c.-82-96_-56del
ENST00000585748.3:c.-82-96_-56del
ENST00000585851.1:c.291-2052_291-1930del	ENSP00000467912.1:n.291-2052_291-1930del
ENST00000585851.2:c.291-2052_291-1930del	ENSP00000467912.2:n.291-2052_291-1930del
ENST00000586243.5:c.291-96_317del
ENST00000586358.5:n.114-96_140del
ENST00000589152.5:n.381-96_407del
ENST00000593219.5:c.*116-96_*142del
ENST00000652231.1:c.291-96_317del
XM_005259617.1:c.291-96_317del
XM_005259617.3:c.291-96_317del
XM_005259618.3:c.291-96_317del
XM_011528209.1:c.69-96_95del
XM_011528209.2:c.69-96_95del
XR_001753738.2:n.916-96_942del
XR_001753739.1:n.916-96_942del
XR_001753740.2:n.916-96_942del
XR_936204.1:n.916-96_942del