Canonical Allele Identifier: CA2611616953
Gene: CYP2E1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133539088dup , CM000672.2:g.133539088dup GRCh38
NC_000010.10:g.135352592dup , CM000672.1:g.135352592dup GRCh37
NC_000010.9:g.135202582dup NCBI36
NG_008383.1:g.16726dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000252945.8:c.*124dup MANE Select ENSP00000252945.3:n.*124dup
ENST00000252945.7:c.*124dup ENSP00000252945.3:n.*124dup
ENST00000368520.1:n.1358+1196dup
ENST00000463117.6:c.*124dup ENSP00000440689.1:n.*124dup
ENST00000469258.1:n.702dup
NM_000773.3:c.*124dup NP_000764.1:n.*124dup
NM_000773.4:c.*124dup MANE Select NP_000764.1:n.*124dup