Canonical Allele Identifier: CA662011558

Gene: CYP2E1

Linked Data

• dbSNP Id: rs1481431795
• MyVariant Identifiers: chr10:g.135352275_135352276insAC (hg19) ; chr10:g.133538771_133538772insAC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.133538772_133538773dup , CM000672.2:g.133538772_133538773dup	GRCh38
NC_000010.10:g.135352276_135352277dup , CM000672.1:g.135352276_135352277dup	GRCh37
NC_000010.9:g.135202266_135202267dup	NCBI36
NG_008383.1:g.16410_16411dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252945.8:c.1298-8_1298-7dup MANE Select	ENSP00000252945.3:n.1298-8_1298-7dup
ENST00000252945.7:c.1298-8_1298-7dup	ENSP00000252945.3:n.1298-8_1298-7dup
ENST00000368520.1:n.1358+880_1358+881dup
ENST00000418356.1:c.887-8_887-7dup	ENSP00000397299.1:n.887-8_887-7dup
ENST00000421586.5:c.1037-8_1037-7dup	ENSP00000412754.1:n.1037-8_1037-7dup
ENST00000463117.6:c.1298-8_1298-7dup	ENSP00000440689.1:n.1298-8_1298-7dup
ENST00000469258.1:n.394-8_394-7dup
ENST00000541080.5:c.714-8_714-7dup
NM_000773.3:c.1298-8_1298-7dup	NP_000764.1:n.1298-8_1298-7dup
NM_000773.4:c.1298-8_1298-7dup MANE Select	NP_000764.1:n.1298-8_1298-7dup