Canonical Allele Identifier: CA2563405705
Gene: NFE2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.54293241del , CM000674.2:g.54293241del GRCh38
NC_000012.11:g.54687025del , CM000674.1:g.54687025del GRCh37
NC_000012.10:g.52973292del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000435572.7:c.257del MANE Select ENSP00000397185.2:p.Pro86GlnfsTer25
ENST00000312156.8:c.257del ENSP00000312436.4:p.Pro86GlnfsTer25
ENST00000435572.6:c.257del ENSP00000397185.2:p.Pro86GlnfsTer25
ENST00000540264.2:c.257del ENSP00000439120.2:p.Pro86GlnfsTer25
ENST00000553070.5:c.257del ENSP00000447558.1:p.Pro86GlnfsTer25
ENST00000553198.1:c.257del ENSP00000446929.1:p.Pro86GlnfsTer25
NM_001136023.2:c.257del NP_001129495.1:p.Pro86GlnfsTer25
NM_001261461.1:c.257del NP_001248390.1:p.Pro86GlnfsTer25
NM_006163.2:c.257del NP_006154.1:p.Pro86GlnfsTer25
XM_005268906.3:c.257del XP_005268963.1:p.Pro86GlnfsTer25
XM_011538397.1:c.224del XP_011536699.1:p.Pro75GlnfsTer25
XM_005268906.4:c.257del XP_005268963.1:p.Pro86GlnfsTer25
NM_001136023.3:c.257del MANE Select NP_001129495.1:p.Pro86GlnfsTer25
NM_001261461.2:c.257del NP_001248390.1:p.Pro86GlnfsTer25
NM_006163.3:c.257del NP_006154.1:p.Pro86GlnfsTer25
NM_001400365.1:c.257del NP_001387294.1:p.Pro86GlnfsTer25
NM_001400372.1:c.-47del NP_001387301.1:n.-47del
NM_001400373.1:c.-47del NP_001387302.1:n.-47del