Canonical Allele Identifier: CA971501079
Gene: CYP1A2 HGNC NCBI

Linked Data

gnomAD v3: 15-74755350-CAA-C
gnomAD v4: 15-74755350-CAA-C
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755360_74755361del , CM000677.2:g.74755360_74755361del GRCh38
NC_000015.9:g.75047701_75047702del , CM000677.1:g.75047701_75047702del GRCh37
NC_000015.8:g.72834754_72834755del NCBI36
NG_008431.1:g.37819_37820del
NG_008431.2:g.37819_37820del
NG_061543.1:g.11516_11517del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*272_*273del MANE Select ENSP00000342007.4:n.*272_*273del
ENST00000343932.4:c.*272_*273del ENSP00000342007.4:n.*272_*273del
NM_000761.4:c.*272_*273del NP_000752.2:n.*272_*273del
NM_000761.5:c.*272_*273del MANE Select NP_000752.2:n.*272_*273del
Search 100 bp 5'
Search 100 bp 3'