Canonical Allele Identifier: CA2573052279
Gene: LEF1 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.108089128del , CM000666.2:g.108089128del GRCh38
NC_000004.11:g.109010284del , CM000666.1:g.109010284del GRCh37
NC_000004.10:g.109229733del NCBI36
NG_015798.1:g.84829del

Transcript Alleles

HGVS Amino-acid Change
ENST00000265165.6:c.544del MANE Select ENSP00000265165.1:p.Gln182LysfsTer?
ENST00000265165.5:c.544del ENSP00000265165.1:p.Gln182LysfsTer?
ENST00000379951.6:c.544del ENSP00000369284.2:p.Gln182LysfsTer?
ENST00000438313.6:c.544del ENSP00000406176.2:p.Gln182LysfsTer?
ENST00000504775.5:n.371del
ENST00000504950.5:c.211-5682del ENSP00000427459.1:n.211-5682del
ENST00000505293.1:n.470del
ENST00000506680.5:c.544del ENSP00000422334.1:p.Gln182LysfsTer?
ENST00000509428.5:n.363del
ENST00000510135.5:n.423del
ENST00000510624.5:c.340del ENSP00000422840.1:p.Gln114LysfsTer?
ENST00000510717.5:n.425del
ENST00000512172.1:c.340del ENSP00000427365.1:p.Gln114LysfsTer?
ENST00000515500.5:c.340del ENSP00000422801.1:p.Gln114LysfsTer?
NM_001130713.2:c.544del NP_001124185.1:p.Gln182LysfsTer?
NM_001130714.2:c.544del NP_001124186.1:p.Gln182LysfsTer?
NM_001166119.1:c.340del NP_001159591.1:p.Gln114LysfsTer?
NM_016269.4:c.544del NP_057353.1:p.Gln182LysfsTer?
XM_005263046.2:c.544del XP_005263103.1:p.Gln182LysfsTer?
XM_005263047.1:c.340del XP_005263104.1:p.Gln114LysfsTer?
XM_005263048.1:c.340del XP_005263105.1:p.Gln114LysfsTer?
XM_006714233.1:c.199del XP_006714296.1:p.Gln67LysfsTer?
XM_005263046.3:c.544del XP_005263103.1:p.Gln182LysfsTer?
NM_016269.5:c.544del MANE Select NP_057353.1:p.Gln182LysfsTer?
NM_001130713.3:c.544del NP_001124185.1:p.Gln182LysfsTer?
NM_001130714.3:c.544del NP_001124186.1:p.Gln182LysfsTer?
NM_001166119.2:c.340del NP_001159591.1:p.Gln114LysfsTer?