Canonical Allele Identifier: CA1946816625
Gene: CYP2E1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133538785C= , CM000672.2:g.133538785C= GRCh38
NC_000010.10:g.135352289C= , CM000672.1:g.135352289C= GRCh37
NC_000010.9:g.135202279C= NCBI36
NG_008383.1:g.16423C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252945.8:c.1303C= MANE Select ENSP00000252945.3:p.Arg435=
ENST00000252945.7:c.1303C= ENSP00000252945.3:p.Arg435=
ENST00000368520.1:n.1358+893C=
ENST00000418356.1:c.892C= ENSP00000397299.1:p.Arg298=
ENST00000421586.5:c.1042C= ENSP00000412754.1:p.Arg348=
ENST00000463117.6:c.1303C= ENSP00000440689.1:p.Arg435=
ENST00000469258.1:n.399C=
ENST00000541080.5:c.719C=
NM_000773.3:c.1303C= NP_000764.1:p.Arg435=
NM_000773.4:c.1303C= MANE Select NP_000764.1:p.Arg435=