Canonical Allele Identifier: CA378835240
Gene: CYP2E1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133532177G>C , CM000672.2:g.133532177G>C GRCh38
NC_000010.10:g.135345681G>C , CM000672.1:g.135345681G>C GRCh37
NC_000010.9:g.135195671G>C NCBI36
NG_008383.1:g.9815G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000252945.8:c.541G>C MANE Select ENSP00000252945.3:p.Ala181Pro
ENST00000252945.7:c.541G>C ENSP00000252945.3:p.Ala181Pro
ENST00000368520.1:n.602G>C
ENST00000418356.1:c.130G>C ENSP00000397299.1:p.Ala44Pro
ENST00000421586.5:c.280G>C ENSP00000412754.1:p.Ala94Pro
ENST00000463117.6:c.541G>C ENSP00000440689.1:p.Ala181Pro
ENST00000477500.5:n.448+443G>C
ENST00000541080.5:c.226+443G>C
NM_000773.3:c.541G>C NP_000764.1:p.Ala181Pro
NM_000773.4:c.541G>C MANE Select NP_000764.1:p.Ala181Pro