Canonical Allele Identifier: CA2611616568

Gene: CYP2E1

Linked Data

• gnomAD v4: 10-133538769-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.133538769G>T , CM000672.2:g.133538769G>T	GRCh38
NC_000010.10:g.135352273G>T , CM000672.1:g.135352273G>T	GRCh37
NC_000010.9:g.135202263G>T	NCBI36
NG_008383.1:g.16407G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252945.8:c.1298-11G>T MANE Select	ENSP00000252945.3:n.1298-11G>T
ENST00000252945.7:c.1298-11G>T	ENSP00000252945.3:n.1298-11G>T
ENST00000368520.1:n.1358+877G>T
ENST00000418356.1:c.887-11G>T	ENSP00000397299.1:n.887-11G>T
ENST00000421586.5:c.1037-11G>T	ENSP00000412754.1:n.1037-11G>T
ENST00000463117.6:c.1298-11G>T	ENSP00000440689.1:n.1298-11G>T
ENST00000469258.1:n.394-11G>T
ENST00000541080.5:c.714-11G>T
NM_000773.3:c.1298-11G>T	NP_000764.1:n.1298-11G>T
NM_000773.4:c.1298-11G>T MANE Select	NP_000764.1:n.1298-11G>T