Canonical Allele Identifier: CA1946816414
Gene: CYP2E1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133538649A= , CM000672.2:g.133538649A= GRCh38
NC_000010.10:g.135352153A= , CM000672.1:g.135352153A= GRCh37
NC_000010.9:g.135202143A= NCBI36
NG_008383.1:g.16287A=

Transcript Alleles

HGVS Amino-acid change
ENST00000252945.8:c.1298-131A= MANE Select ENSP00000252945.3:n.1298-131A=
ENST00000252945.7:c.1298-131A= ENSP00000252945.3:n.1298-131A=
ENST00000368520.1:n.1358+757A=
ENST00000418356.1:c.887-131A= ENSP00000397299.1:n.887-131A=
ENST00000421586.5:c.1037-131A= ENSP00000412754.1:n.1037-131A=
ENST00000463117.6:c.1298-131A= ENSP00000440689.1:n.1298-131A=
ENST00000469258.1:n.394-131A=
ENST00000541080.5:c.714-131A=
NM_000773.3:c.1298-131A= NP_000764.1:n.1298-131A=
NM_000773.4:c.1298-131A= MANE Select NP_000764.1:n.1298-131A=