Canonical Allele Identifier: CA1946816641
Gene: CYP2E1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133538790G= , CM000672.2:g.133538790G= GRCh38
NC_000010.10:g.135352294G= , CM000672.1:g.135352294G= GRCh37
NC_000010.9:g.135202284G= NCBI36
NG_008383.1:g.16428G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252945.8:c.1308G= MANE Select ENSP00000252945.3:p.Val436=
ENST00000252945.7:c.1308G= ENSP00000252945.3:p.Val436=
ENST00000368520.1:n.1358+898G=
ENST00000418356.1:c.897G= ENSP00000397299.1:p.Val299=
ENST00000421586.5:c.1047G= ENSP00000412754.1:p.Val349=
ENST00000463117.6:c.1308G= ENSP00000440689.1:p.Val436=
ENST00000469258.1:n.404G=
ENST00000541080.5:c.724G=
NM_000773.3:c.1308G= NP_000764.1:p.Val436=
NM_000773.4:c.1308G= MANE Select NP_000764.1:p.Val436=