Canonical Allele Identifier: CA480094539

Gene: NFE2

Linked Data

• gnomAD v4: 12-54293094-C-T
• MyVariant Identifiers: chr12:g.54686878C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.54293094C>T , CM000674.2:g.54293094C>T	GRCh38
NC_000012.11:g.54686878C>T , CM000674.1:g.54686878C>T	GRCh37
NC_000012.10:g.52973145C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435572.7:c.402G>A MANE Select	ENSP00000397185.2:p.Gly134=
ENST00000312156.8:c.402G>A	ENSP00000312436.4:p.Gly134=
ENST00000435572.6:c.402G>A	ENSP00000397185.2:p.Gly134=
ENST00000540264.2:c.402G>A	ENSP00000439120.2:p.Gly134=
ENST00000553070.5:c.402G>A	ENSP00000447558.1:p.Gly134=
ENST00000553198.1:c.402G>A	ENSP00000446929.1:p.Gly134=
NM_001136023.2:c.402G>A	NP_001129495.1:p.Gly134=
NM_001261461.1:c.402G>A	NP_001248390.1:p.Gly134=
NM_006163.2:c.402G>A	NP_006154.1:p.Gly134=
XM_005268906.3:c.402G>A	XP_005268963.1:p.Gly134=
XM_011538397.1:c.369G>A	XP_011536699.1:p.Gly123=
XM_005268906.4:c.402G>A	XP_005268963.1:p.Gly134=
NM_001136023.3:c.402G>A MANE Select	NP_001129495.1:p.Gly134=
NM_001261461.2:c.402G>A	NP_001248390.1:p.Gly134=
NM_006163.3:c.402G>A	NP_006154.1:p.Gly134=
NM_001400365.1:c.402G>A	NP_001387294.1:p.Gly134=
NM_001400372.1:c.99G>A	NP_001387301.1:p.Gly33=
NM_001400373.1:c.99G>A	NP_001387302.1:p.Gly33=