Canonical Allele Identifier: CA1946829912
Gene: CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs1851343740

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133531976_133531979del , CM000672.2:g.133531976_133531979del GRCh38
NC_000010.10:g.135345480_135345483del , CM000672.1:g.135345480_135345483del GRCh37
NC_000010.9:g.135195470_135195473del NCBI36
NG_008383.1:g.9614_9617del

Transcript Alleles

HGVS Amino-acid Change
ENST00000252945.8:c.488-148_488-145del MANE Select ENSP00000252945.3:n.488-148_488-145del
ENST00000252945.7:c.488-148_488-145del ENSP00000252945.3:n.488-148_488-145del
ENST00000368520.1:n.401_404del
ENST00000418356.1:c.77-148_77-145del ENSP00000397299.1:n.77-148_77-145del
ENST00000421586.5:c.227-148_227-145del ENSP00000412754.1:n.227-148_227-145del
ENST00000463117.6:c.488-148_488-145del ENSP00000440689.1:n.488-148_488-145del
ENST00000477500.5:n.448+242_448+245del
ENST00000480558.1:n.713-148_713-145del
ENST00000541080.5:c.226+242_226+245del
NM_000773.3:c.488-148_488-145del NP_000764.1:n.488-148_488-145del
NM_000773.4:c.488-148_488-145del MANE Select NP_000764.1:n.488-148_488-145del