Canonical Allele Identifier: CA2838406299

Gene: NFE2L2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.177364654C>A , CM000664.2:g.177364654C>A	GRCh38
NC_000002.11:g.178229382C>A , CM000664.1:g.178229382C>A	GRCh37
NC_000002.10:g.177937628C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699265.1:c.-365-25955G>T	ENSP00000514246.1:n.-365-25955G>T
ENST00000699301.1:c.-677-25955G>T	ENSP00000514281.1:n.-677-25955G>T
ENST00000699303.1:c.-476+20632G>T	ENSP00000514283.1:n.-476+20632G>T
ENST00000699304.1:c.-523-25955G>T	ENSP00000514284.1:n.-523-25955G>T
ENST00000699305.1:c.-458-25955G>T	ENSP00000514285.1:n.-458-25955G>T
ENST00000699331.1:c.-633-25955G>T	ENSP00000514305.1:n.-633-25955G>T
ENST00000699344.1:c.-523-25955G>T	ENSP00000514319.1:n.-523-25955G>T
ENST00000699345.1:c.-455-25955G>T	ENSP00000514320.1:n.-455-25955G>T
ENST00000699346.1:c.-520-25955G>T	ENSP00000514321.1:n.-520-25955G>T
ENST00000699348.1:c.-264+27919G>T	ENSP00000514323.1:n.-264+27919G>T
ENST00000699406.1:c.-630-25955G>T	ENSP00000514367.1:n.-630-25955G>T
ENST00000699408.1:c.-828-25955G>T	ENSP00000514369.1:n.-828-25955G>T
ENST00000699409.1:c.-720+20632G>T	ENSP00000514370.1:n.-720+20632G>T
ENST00000699410.1:c.-124+27919G>T	ENSP00000514371.1:n.-124+27919G>T
ENST00000699411.1:c.-365-25955G>T	ENSP00000514372.1:n.-365-25955G>T
ENST00000699412.1:c.-455-25955G>T	ENSP00000514373.1:n.-455-25955G>T
ENST00000699413.1:n.113-25955G>T
ENST00000699414.1:n.113-25955G>T
ENST00000699434.1:c.-576-25955G>T	ENSP00000514386.1:n.-576-25955G>T
ENST00000699435.1:c.-576+27919G>T	ENSP00000514387.1:n.-576+27919G>T
ENST00000464747.5:c.-377-25955G>T	ENSP00000467401.1:n.-377-25955G>T
NR_026966.1:n.120-25955G>T