Canonical Allele Identifier: CA1946816559

Gene: CYP2E1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.133538730G= , CM000672.2:g.133538730G=	GRCh38
NC_000010.10:g.135352234G= , CM000672.1:g.135352234G=	GRCh37
NC_000010.9:g.135202224G=	NCBI36
NG_008383.1:g.16368G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252945.8:c.1298-50G= MANE Select	ENSP00000252945.3:n.1298-50G=
ENST00000252945.7:c.1298-50G=	ENSP00000252945.3:n.1298-50G=
ENST00000368520.1:n.1358+838G=
ENST00000418356.1:c.887-50G=	ENSP00000397299.1:n.887-50G=
ENST00000421586.5:c.1037-50G=	ENSP00000412754.1:n.1037-50G=
ENST00000463117.6:c.1298-50G=	ENSP00000440689.1:n.1298-50G=
ENST00000469258.1:n.394-50G=
ENST00000541080.5:c.714-50G=
NM_000773.3:c.1298-50G=	NP_000764.1:n.1298-50G=
NM_000773.4:c.1298-50G= MANE Select	NP_000764.1:n.1298-50G=