Canonical Allele Identifier: CA378835226
Gene: CYP2E1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133532174A>T , CM000672.2:g.133532174A>T GRCh38
NC_000010.10:g.135345678A>T , CM000672.1:g.135345678A>T GRCh37
NC_000010.9:g.135195668A>T NCBI36
NG_008383.1:g.9812A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000252945.8:c.538A>T MANE Select ENSP00000252945.3:p.Ile180Leu
ENST00000252945.7:c.538A>T ENSP00000252945.3:p.Ile180Leu
ENST00000368520.1:n.599A>T
ENST00000418356.1:c.127A>T ENSP00000397299.1:p.Ile43Leu
ENST00000421586.5:c.277A>T ENSP00000412754.1:p.Ile93Leu
ENST00000463117.6:c.538A>T ENSP00000440689.1:p.Ile180Leu
ENST00000477500.5:n.448+440A>T
ENST00000541080.5:c.226+440A>T
NM_000773.3:c.538A>T NP_000764.1:p.Ile180Leu
NM_000773.4:c.538A>T MANE Select NP_000764.1:p.Ile180Leu