Canonical Allele Identifier: CA2629512214
Gene: CYP1A2 HGNC NCBI

Linked Data

gnomAD v4: 15-74755356-AAAAAAC-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755360_74755365del , CM000677.2:g.74755360_74755365del GRCh38
NC_000015.9:g.75047701_75047706del , CM000677.1:g.75047701_75047706del GRCh37
NC_000015.8:g.72834754_72834759del NCBI36
NG_008431.1:g.37819_37824del
NG_008431.2:g.37819_37824del
NG_061543.1:g.11516_11521del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*272_*277del MANE Select ENSP00000342007.4:n.*272_*277del
ENST00000343932.4:c.*272_*277del ENSP00000342007.4:n.*272_*277del
NM_000761.4:c.*272_*277del NP_000752.2:n.*272_*277del
NM_000761.5:c.*272_*277del MANE Select NP_000752.2:n.*272_*277del
Search 100 bp 5'
Search 100 bp 3'