Canonical Allele Identifier: CA479990375

Gene: NFE2

Linked Data

• dbSNP Id: rs1592179477
• MyVariant Identifiers: chr12:g.54687040T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.54293256T>G , CM000674.2:g.54293256T>G	GRCh38
NC_000012.11:g.54687040T>G , CM000674.1:g.54687040T>G	GRCh37
NC_000012.10:g.52973307T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000435572.7:c.240A>C MANE Select	ENSP00000397185.2:p.Pro80=
ENST00000312156.8:c.240A>C	ENSP00000312436.4:p.Pro80=
ENST00000435572.6:c.240A>C	ENSP00000397185.2:p.Pro80=
ENST00000540264.2:c.240A>C	ENSP00000439120.2:p.Pro80=
ENST00000553070.5:c.240A>C	ENSP00000447558.1:p.Pro80=
ENST00000553198.1:c.240A>C	ENSP00000446929.1:p.Pro80=
NM_001136023.2:c.240A>C	NP_001129495.1:p.Pro80=
NM_001261461.1:c.240A>C	NP_001248390.1:p.Pro80=
NM_006163.2:c.240A>C	NP_006154.1:p.Pro80=
XM_005268906.3:c.240A>C	XP_005268963.1:p.Pro80=
XM_011538397.1:c.207A>C	XP_011536699.1:p.Pro69=
XM_005268906.4:c.240A>C	XP_005268963.1:p.Pro80=
NM_001136023.3:c.240A>C MANE Select	NP_001129495.1:p.Pro80=
NM_001261461.2:c.240A>C	NP_001248390.1:p.Pro80=
NM_006163.3:c.240A>C	NP_006154.1:p.Pro80=
NM_001400365.1:c.240A>C	NP_001387294.1:p.Pro80=
NM_001400372.1:c.-64A>C	NP_001387301.1:n.-64A>C
NM_001400373.1:c.-64A>C	NP_001387302.1:n.-64A>C