Canonical Allele Identifier: CA2629512132
Gene: CYP1A2 HGNC NCBI

Linked Data

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

HGVS Genome Assembly
NC_000015.10:g.74755298_74755299insA , CM000677.2:g.74755298_74755299insA GRCh38
NC_000015.9:g.75047639_75047640insA , CM000677.1:g.75047639_75047640insA GRCh37
NC_000015.8:g.72834692_72834693insA NCBI36
NG_008431.1:g.37757_37758insA
NG_008431.2:g.37757_37758insA
NG_061543.1:g.11454_11455insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*210_*211insA MANE Select ENSP00000342007.4:n.*210_*211insA
ENST00000343932.4:c.*210_*211insA ENSP00000342007.4:n.*210_*211insA
NM_000761.4:c.*210_*211insA NP_000752.2:n.*210_*211insA
NM_000761.5:c.*210_*211insA MANE Select NP_000752.2:n.*210_*211insA
Search 100 bp 5'
Search 100 bp 3'