Canonical Allele Identifier: CA1946830252

Gene: CYP2E1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.133532189T= , CM000672.2:g.133532189T=	GRCh38
NC_000010.10:g.135345693T= , CM000672.1:g.135345693T=	GRCh37
NC_000010.9:g.135195683T=	NCBI36
NG_008383.1:g.9827T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000252945.8:c.553T= MANE Select	ENSP00000252945.3:p.Phe185=
ENST00000252945.7:c.553T=	ENSP00000252945.3:p.Phe185=
ENST00000368520.1:n.614T=
ENST00000418356.1:c.142T=	ENSP00000397299.1:p.Phe48=
ENST00000421586.5:c.292T=	ENSP00000412754.1:p.Phe98=
ENST00000463117.6:c.553T=	ENSP00000440689.1:p.Phe185=
ENST00000477500.5:n.448+455T=
ENST00000541080.5:c.226+455T=
NM_000773.3:c.553T=	NP_000764.1:p.Phe185=
NM_000773.4:c.553T= MANE Select	NP_000764.1:p.Phe185=