Canonical Allele Identifier: CA2580965075
Gene: CYP2E1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133532099G>C , CM000672.2:g.133532099G>C GRCh38
NC_000010.10:g.135345603G>C , CM000672.1:g.135345603G>C GRCh37
NC_000010.9:g.135195593G>C NCBI36
NG_008383.1:g.9737G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252945.8:c.488-25G>C MANE Select ENSP00000252945.3:n.488-25G>C
ENST00000252945.7:c.488-25G>C ENSP00000252945.3:n.488-25G>C
ENST00000368520.1:n.524G>C
ENST00000418356.1:c.77-25G>C ENSP00000397299.1:n.77-25G>C
ENST00000421586.5:c.227-25G>C ENSP00000412754.1:n.227-25G>C
ENST00000463117.6:c.488-25G>C ENSP00000440689.1:n.488-25G>C
ENST00000477500.5:n.448+365G>C
ENST00000480558.1:n.713-25G>C
ENST00000541080.5:c.226+365G>C
NM_000773.3:c.488-25G>C NP_000764.1:n.488-25G>C
NM_000773.4:c.488-25G>C MANE Select NP_000764.1:n.488-25G>C