Canonical Allele Identifier: CA2830556605
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74750269_74750270del , CM000677.2:g.74750269_74750270del GRCh38
NC_000015.9:g.75042610_75042611del , CM000677.1:g.75042610_75042611del GRCh37
NC_000015.8:g.72829663_72829664del NCBI36
NG_008431.1:g.32728_32729del
NG_008431.2:g.32728_32729del
NG_061543.1:g.6425_6426del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.531_532del MANE Select ENSP00000342007.4:p.Glu178AlafsTer?
ENST00000343932.4:c.531_532del ENSP00000342007.4:p.Glu178AlafsTer?
NM_000761.4:c.531_532del NP_000752.2:p.Glu178AlafsTer?
NM_000761.5:c.531_532del MANE Select NP_000752.2:p.Glu178AlafsTer?