Canonical Allele Identifier: CA1946814999
Gene: CYP2E1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133537633G= , CM000672.2:g.133537633G= GRCh38
NC_000010.10:g.135351137G= , CM000672.1:g.135351137G= GRCh37
NC_000010.9:g.135201127G= NCBI36
NG_008383.1:g.15271G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252945.8:c.1156-118G= MANE Select ENSP00000252945.3:n.1156-118G=
ENST00000252945.7:c.1156-118G= ENSP00000252945.3:n.1156-118G=
ENST00000368520.1:n.1217-118G=
ENST00000418356.1:c.745-118G= ENSP00000397299.1:n.745-118G=
ENST00000421586.5:c.895-118G= ENSP00000412754.1:n.895-118G=
ENST00000463117.6:c.1156-118G= ENSP00000440689.1:n.1156-118G=
ENST00000469258.1:n.134G=
ENST00000541080.5:c.572-118G=
NM_000773.3:c.1156-118G= NP_000764.1:n.1156-118G=
NM_000773.4:c.1156-118G= MANE Select NP_000764.1:n.1156-118G=