Canonical Allele Identifier: CA2187824771
Gene: CYP1A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74750175_74750178delinsCCTT , CM000677.2:g.74750175_74750178delinsCCTT GRCh38
NC_000015.9:g.75042516_75042519delinsCCTT , CM000677.1:g.75042516_75042519delinsCCTT GRCh37
NC_000015.8:g.72829569_72829572delinsCCTT NCBI36
NG_008431.1:g.32634_32637delinsCCTT
NG_008431.2:g.32634_32637delinsCCTT
NG_061543.1:g.6331_6334delinsCCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.437_440delinsCCTT MANE Select ENSP00000342007.4:p.Thr146=
ENST00000343932.4:c.437_440delinsCCTT ENSP00000342007.4:p.Thr146=
NM_000761.4:c.437_440delinsCCTT NP_000752.2:p.Thr146=
NM_000761.5:c.437_440delinsCCTT MANE Select NP_000752.2:p.Thr146=
Search 100 bp 5'
Search 100 bp 3'