Canonical Allele Identifier: CA2611616715
Gene: CYP2E1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133532178_133532179dup , CM000672.2:g.133532178_133532179dup GRCh38
NC_000010.10:g.135345682_135345683dup , CM000672.1:g.135345682_135345683dup GRCh37
NC_000010.9:g.135195672_135195673dup NCBI36
NG_008383.1:g.9816_9817dup

Transcript Alleles

HGVS Amino-acid change
ENST00000252945.8:c.542_543dup MANE Select ENSP00000252945.3:p.Asp182ProfsTer17
ENST00000252945.7:c.542_543dup ENSP00000252945.3:p.Asp182ProfsTer17
ENST00000368520.1:n.603_604dup
ENST00000418356.1:c.131_132dup ENSP00000397299.1:p.Asp45ProfsTer17
ENST00000421586.5:c.281_282dup ENSP00000412754.1:p.Asp95ProfsTer17
ENST00000463117.6:c.542_543dup ENSP00000440689.1:p.Asp182ProfsTer17
ENST00000477500.5:n.448+444_448+445dup
ENST00000541080.5:c.226+444_226+445dup
NM_000773.3:c.542_543dup NP_000764.1:p.Asp182ProfsTer17
NM_000773.4:c.542_543dup MANE Select NP_000764.1:p.Asp182ProfsTer17