Canonical Allele Identifier: CA378835291
Gene: CYP2E1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133532183A>T , CM000672.2:g.133532183A>T GRCh38
NC_000010.10:g.135345687A>T , CM000672.1:g.135345687A>T GRCh37
NC_000010.9:g.135195677A>T NCBI36
NG_008383.1:g.9821A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000252945.8:c.547A>T MANE Select ENSP00000252945.3:p.Ile183Phe
ENST00000252945.7:c.547A>T ENSP00000252945.3:p.Ile183Phe
ENST00000368520.1:n.608A>T
ENST00000418356.1:c.136A>T ENSP00000397299.1:p.Ile46Phe
ENST00000421586.5:c.286A>T ENSP00000412754.1:p.Ile96Phe
ENST00000463117.6:c.547A>T ENSP00000440689.1:p.Ile183Phe
ENST00000477500.5:n.448+449A>T
ENST00000541080.5:c.226+449A>T
NM_000773.3:c.547A>T NP_000764.1:p.Ile183Phe
NM_000773.4:c.547A>T MANE Select NP_000764.1:p.Ile183Phe