Canonical Allele Identifier: CA2629512129
Gene: CYP1A2 HGNC NCBI

Linked Data

gnomAD v4: 15-74755298-C-CAA
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755298_74755299insAA , CM000677.2:g.74755298_74755299insAA GRCh38
NC_000015.9:g.75047639_75047640insAA , CM000677.1:g.75047639_75047640insAA GRCh37
NC_000015.8:g.72834692_72834693insAA NCBI36
NG_008431.1:g.37757_37758insAA
NG_008431.2:g.37757_37758insAA
NG_061543.1:g.11454_11455insAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*210_*211insAA MANE Select ENSP00000342007.4:n.*210_*211insAA
ENST00000343932.4:c.*210_*211insAA ENSP00000342007.4:n.*210_*211insAA
NM_000761.4:c.*210_*211insAA NP_000752.2:n.*210_*211insAA
NM_000761.5:c.*210_*211insAA MANE Select NP_000752.2:n.*210_*211insAA
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