Canonical Allele Identifier: CA2187827292

Gene: CYP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74755348_74755349delinsCT , CM000677.2:g.74755348_74755349delinsCT	GRCh38
NC_000015.9:g.75047689_75047690delinsCT , CM000677.1:g.75047689_75047690delinsCT	GRCh37
NC_000015.8:g.72834742_72834743delinsCT	NCBI36
NG_008431.1:g.37807_37808delinsCT
NG_008431.2:g.37807_37808delinsCT
NG_061543.1:g.11504_11505delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.*260_*261delinsCT MANE Select	ENSP00000342007.4:n.*260_*261delinsCT
ENST00000343932.4:c.*260_*261delinsCT	ENSP00000342007.4:n.*260_*261delinsCT
NM_000761.4:c.*260_*261delinsCT	NP_000752.2:n.*260_*261delinsCT
NM_000761.5:c.*260_*261delinsCT MANE Select	NP_000752.2:n.*260_*261delinsCT