Canonical Allele Identifier: CA2037368064
Gene: NFE2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.54293482A= , CM000674.2:g.54293482A= GRCh38
NC_000012.11:g.54687266A= , CM000674.1:g.54687266A= GRCh37
NC_000012.10:g.52973533A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000435572.7:c.115-101T= MANE Select ENSP00000397185.2:n.115-101T=
ENST00000312156.8:c.115-101T= ENSP00000312436.4:n.115-101T=
ENST00000435572.6:c.115-101T= ENSP00000397185.2:n.115-101T=
ENST00000540264.2:c.115-101T= ENSP00000439120.2:n.115-101T=
ENST00000553070.5:c.115-101T= ENSP00000447558.1:n.115-101T=
ENST00000553198.1:c.115-101T= ENSP00000446929.1:n.115-101T=
NM_001136023.2:c.115-101T= NP_001129495.1:n.115-101T=
NM_001261461.1:c.115-101T= NP_001248390.1:n.115-101T=
NM_006163.2:c.115-101T= NP_006154.1:n.115-101T=
XM_005268906.3:c.115-101T= XP_005268963.1:n.115-101T=
XM_011538397.1:c.82-101T= XP_011536699.1:n.82-101T=
XM_005268906.4:c.115-101T= XP_005268963.1:n.115-101T=
NM_001136023.3:c.115-101T= MANE Select NP_001129495.1:n.115-101T=
NM_001261461.2:c.115-101T= NP_001248390.1:n.115-101T=
NM_006163.3:c.115-101T= NP_006154.1:n.115-101T=
NM_001400365.1:c.115-101T= NP_001387294.1:n.115-101T=
NM_001400372.1:c.-189-101T= NP_001387301.1:n.-189-101T=
NM_001400373.1:c.-189-101T= NP_001387302.1:n.-189-101T=