Canonical Allele Identifier: CA2611616533

Gene: CYP2E1

Linked Data

• gnomAD v4: 10-133538747-T-TCTGAAACTGTTAA

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.133538748_133538749insTGAAACTGTTAAC , CM000672.2:g.133538748_133538749insTGAAACTGTTAAC	GRCh38
NC_000010.10:g.135352252_135352253insTGAAACTGTTAAC , CM000672.1:g.135352252_135352253insTGAAACTGTTAAC	GRCh37
NC_000010.9:g.135202242_135202243insTGAAACTGTTAAC	NCBI36
NG_008383.1:g.16386_16387insTGAAACTGTTAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252945.8:c.1298-32_1298-31insTGAAACTGTTAAC MANE Select	ENSP00000252945.3:n.1298-32_1298-31insTGAAACTGTTAAC
ENST00000252945.7:c.1298-32_1298-31insTGAAACTGTTAAC	ENSP00000252945.3:n.1298-32_1298-31insTGAAACTGTTAAC
ENST00000368520.1:n.1358+856_1358+857insTGAAACTGTTAAC
ENST00000418356.1:c.887-32_887-31insTGAAACTGTTAAC	ENSP00000397299.1:n.887-32_887-31insTGAAACTGTTAAC
ENST00000421586.5:c.1037-32_1037-31insTGAAACTGTTAAC	ENSP00000412754.1:n.1037-32_1037-31insTGAAACTGTTAAC
ENST00000463117.6:c.1298-32_1298-31insTGAAACTGTTAAC	ENSP00000440689.1:n.1298-32_1298-31insTGAAACTGTTAAC
ENST00000469258.1:n.394-32_394-31insTGAAACTGTTAAC
ENST00000541080.5:c.714-32_714-31insTGAAACTGTTAAC
NM_000773.3:c.1298-32_1298-31insTGAAACTGTTAAC	NP_000764.1:n.1298-32_1298-31insTGAAACTGTTAAC
NM_000773.4:c.1298-32_1298-31insTGAAACTGTTAAC MANE Select	NP_000764.1:n.1298-32_1298-31insTGAAACTGTTAAC