Canonical Allele Identifier: CA2611616570
Gene: CYP2E1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133532072_133532075del , CM000672.2:g.133532072_133532075del GRCh38
NC_000010.10:g.135345576_135345579del , CM000672.1:g.135345576_135345579del GRCh37
NC_000010.9:g.135195566_135195569del NCBI36
NG_008383.1:g.9710_9713del

Transcript Alleles

HGVS Amino-acid change
ENST00000252945.8:c.488-52_488-49del MANE Select ENSP00000252945.3:n.488-52_488-49del
ENST00000252945.7:c.488-52_488-49del ENSP00000252945.3:n.488-52_488-49del
ENST00000368520.1:n.497_500del
ENST00000418356.1:c.77-52_77-49del ENSP00000397299.1:n.77-52_77-49del
ENST00000421586.5:c.227-52_227-49del ENSP00000412754.1:n.227-52_227-49del
ENST00000463117.6:c.488-52_488-49del ENSP00000440689.1:n.488-52_488-49del
ENST00000477500.5:n.448+338_448+341del
ENST00000480558.1:n.713-52_713-49del
ENST00000541080.5:c.226+338_226+341del
NM_000773.3:c.488-52_488-49del NP_000764.1:n.488-52_488-49del
NM_000773.4:c.488-52_488-49del MANE Select NP_000764.1:n.488-52_488-49del