Canonical Allele Identifier: CA2575178103
Gene: NFE2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.54293261del , CM000674.2:g.54293261del GRCh38
NC_000012.11:g.54687045del , CM000674.1:g.54687045del GRCh37
NC_000012.10:g.52973312del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000435572.7:c.236del MANE Select ENSP00000397185.2:p.Pro79LeufsTer?
ENST00000312156.8:c.236del ENSP00000312436.4:p.Pro79LeufsTer?
ENST00000435572.6:c.236del ENSP00000397185.2:p.Pro79LeufsTer?
ENST00000540264.2:c.236del ENSP00000439120.2:p.Pro79LeufsTer?
ENST00000553070.5:c.236del ENSP00000447558.1:p.Pro79LeufsTer?
ENST00000553198.1:c.236del ENSP00000446929.1:p.Pro79LeufsTer?
NM_001136023.2:c.236del NP_001129495.1:p.Pro79LeufsTer?
NM_001261461.1:c.236del NP_001248390.1:p.Pro79LeufsTer?
NM_006163.2:c.236del NP_006154.1:p.Pro79LeufsTer?
XM_005268906.3:c.236del XP_005268963.1:p.Pro79LeufsTer?
XM_011538397.1:c.203del XP_011536699.1:p.Pro68LeufsTer?
XM_005268906.4:c.236del XP_005268963.1:p.Pro79LeufsTer?
NM_001136023.3:c.236del MANE Select NP_001129495.1:p.Pro79LeufsTer?
NM_001261461.2:c.236del NP_001248390.1:p.Pro79LeufsTer?
NM_006163.3:c.236del NP_006154.1:p.Pro79LeufsTer?
NM_001400365.1:c.236del NP_001387294.1:p.Pro79LeufsTer?
NM_001400372.1:c.-68del NP_001387301.1:n.-68del
NM_001400373.1:c.-68del NP_001387302.1:n.-68del