Canonical Allele Identifier: CA2573155751

Gene: STK11

Linked Data

• dbSNP Id: rs2145420803

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218482_1218501del , CM000681.2:g.1218482_1218501del	GRCh38
NC_000019.9:g.1218481_1218500del , CM000681.1:g.1218481_1218500del	GRCh37
NC_000019.8:g.1169481_1169500del	NCBI36
NG_007460.2:g.34076_34095del , LRG_319:g.34076_34095del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.356_374+1del
ENST00000585748.3:c.-17_2+1del
ENST00000585851.2:c.291-1891_291-1872del	ENSP00000467912.2:n.291-1891_291-1872del
ENST00000326873.12:c.356_374+1del
ENST00000652231.1:c.356_374+1del
ENST00000326873.11:c.356_374+1del
ENST00000585748.2:c.-17_2+1del
ENST00000585851.1:c.291-1891_291-1872del	ENSP00000467912.1:n.291-1891_291-1872del
ENST00000586243.5:c.356_374+1del
ENST00000586358.5:n.179_197+1del
ENST00000589152.5:n.446_464+1del
ENST00000593219.5:c.*181_*199+1del
NM_000455.4:c.356_374+1del , LRG_319t1:c.356_374+1del
XM_005259617.1:c.356_374+1del
XM_005259618.3:c.356_374+1del
XM_011528209.1:c.134_152+1del
XR_936204.1:n.981_999+1del
XM_005259617.3:c.356_374+1del
XM_011528209.2:c.134_152+1del
XR_001753738.2:n.981_999+1del
XR_001753739.1:n.981_999+1del
XR_001753740.2:n.981_999+1del
NM_000455.5:c.356_374+1del