Canonical Allele Identifier: CA2838302081
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74750058dup , CM000677.2:g.74750058dup GRCh38
NC_000015.9:g.75042399dup , CM000677.1:g.75042399dup GRCh37
NC_000015.8:g.72829452dup NCBI36
NG_008431.1:g.32517dup
NG_008431.2:g.32517dup
NG_061543.1:g.6214dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.320dup MANE Select ENSP00000342007.4:p.Arg108ProfsTer3
ENST00000343932.4:c.320dup ENSP00000342007.4:p.Arg108ProfsTer3
NM_000761.4:c.320dup NP_000752.2:p.Arg108ProfsTer3
NM_000761.5:c.320dup MANE Select NP_000752.2:p.Arg108ProfsTer3