Canonical Allele Identifier: CA1946829913
Gene: CYP2E1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133531977A= , CM000672.2:g.133531977A= GRCh38
NC_000010.10:g.135345481A= , CM000672.1:g.135345481A= GRCh37
NC_000010.9:g.135195471A= NCBI36
NG_008383.1:g.9615A=

Transcript Alleles

HGVS Amino-acid change
ENST00000252945.8:c.488-147A= MANE Select ENSP00000252945.3:n.488-147A=
ENST00000252945.7:c.488-147A= ENSP00000252945.3:n.488-147A=
ENST00000368520.1:n.402A=
ENST00000418356.1:c.77-147A= ENSP00000397299.1:n.77-147A=
ENST00000421586.5:c.227-147A= ENSP00000412754.1:n.227-147A=
ENST00000463117.6:c.488-147A= ENSP00000440689.1:n.488-147A=
ENST00000477500.5:n.448+243A=
ENST00000480558.1:n.713-147A=
ENST00000541080.5:c.226+243A=
NM_000773.3:c.488-147A= NP_000764.1:n.488-147A=
NM_000773.4:c.488-147A= MANE Select NP_000764.1:n.488-147A=