Canonical Allele Identifier: CA6606629
Gene: NFE2 HGNC NCBI

Linked Data

dbSNP Id: rs746688020

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.54293341G>A , CM000674.2:g.54293341G>A GRCh38
NC_000012.11:g.54687125G>A , CM000674.1:g.54687125G>A GRCh37
NC_000012.10:g.52973392G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000435572.7:c.155C>T MANE Select ENSP00000397185.2:p.Ala52Val
ENST00000312156.8:c.155C>T ENSP00000312436.4:p.Ala52Val
ENST00000435572.6:c.155C>T ENSP00000397185.2:p.Ala52Val
ENST00000540264.2:c.155C>T ENSP00000439120.2:p.Ala52Val
ENST00000553070.5:c.155C>T ENSP00000447558.1:p.Ala52Val
ENST00000553198.1:c.155C>T ENSP00000446929.1:p.Ala52Val
NM_001136023.2:c.155C>T NP_001129495.1:p.Ala52Val
NM_001261461.1:c.155C>T NP_001248390.1:p.Ala52Val
NM_006163.2:c.155C>T NP_006154.1:p.Ala52Val
XM_005268906.3:c.155C>T XP_005268963.1:p.Ala52Val
XM_011538397.1:c.122C>T XP_011536699.1:p.Ala41Val
XM_005268906.4:c.155C>T XP_005268963.1:p.Ala52Val
NM_001136023.3:c.155C>T MANE Select NP_001129495.1:p.Ala52Val
NM_001261461.2:c.155C>T NP_001248390.1:p.Ala52Val
NM_006163.3:c.155C>T NP_006154.1:p.Ala52Val
NM_001400365.1:c.155C>T NP_001387294.1:p.Ala52Val
NM_001400372.1:c.-149C>T NP_001387301.1:n.-149C>T
NM_001400373.1:c.-149C>T NP_001387302.1:n.-149C>T