Canonical Allele Identifier: CA1946816634
Gene: CYP2E1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133538787A= , CM000672.2:g.133538787A= GRCh38
NC_000010.10:g.135352291A= , CM000672.1:g.135352291A= GRCh37
NC_000010.9:g.135202281A= NCBI36
NG_008383.1:g.16425A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252945.8:c.1305A= MANE Select ENSP00000252945.3:p.Arg435=
ENST00000252945.7:c.1305A= ENSP00000252945.3:p.Arg435=
ENST00000368520.1:n.1358+895A=
ENST00000418356.1:c.894A= ENSP00000397299.1:p.Arg298=
ENST00000421586.5:c.1044A= ENSP00000412754.1:p.Arg348=
ENST00000463117.6:c.1305A= ENSP00000440689.1:p.Arg435=
ENST00000469258.1:n.401A=
ENST00000541080.5:c.721A=
NM_000773.3:c.1305A= NP_000764.1:p.Arg435=
NM_000773.4:c.1305A= MANE Select NP_000764.1:p.Arg435=