Canonical Allele Identifier: CA1946830194
Gene: CYP2E1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133532169_133532177delinsACGTCATAG , CM000672.2:g.133532169_133532177delinsACGTCATAG GRCh38
NC_000010.10:g.135345673_135345681delinsACGTCATAG , CM000672.1:g.135345673_135345681delinsACGTCATAG GRCh37
NC_000010.9:g.135195663_135195671delinsACGTCATAG NCBI36
NG_008383.1:g.9807_9815delinsACGTCATAG

Transcript Alleles

HGVS Amino-acid change
ENST00000252945.8:c.533_541delinsACGTCATAG MANE Select ENSP00000252945.3:p.Asn178=
ENST00000252945.7:c.533_541delinsACGTCATAG ENSP00000252945.3:p.Asn178=
ENST00000368520.1:n.594_602delinsACGTCATAG
ENST00000418356.1:c.122_130delinsACGTCATAG ENSP00000397299.1:p.Asn41=
ENST00000421586.5:c.272_280delinsACGTCATAG ENSP00000412754.1:p.Asn91=
ENST00000463117.6:c.533_541delinsACGTCATAG ENSP00000440689.1:p.Asn178=
ENST00000477500.5:n.448+435_448+443delinsACGTCATAG
ENST00000541080.5:c.226+435_226+443delinsACGTCATAG
NM_000773.3:c.533_541delinsACGTCATAG NP_000764.1:p.Asn178=
NM_000773.4:c.533_541delinsACGTCATAG MANE Select NP_000764.1:p.Asn178=