Canonical Allele Identifier: CA2629512217

Gene: CYP1A2

Linked Data

• gnomAD v4: 15-74755358-A-AAAC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74755360_74755361insCAA , CM000677.2:g.74755360_74755361insCAA	GRCh38
NC_000015.9:g.75047701_75047702insCAA , CM000677.1:g.75047701_75047702insCAA	GRCh37
NC_000015.8:g.72834754_72834755insCAA	NCBI36
NG_008431.1:g.37819_37820insCAA
NG_008431.2:g.37819_37820insCAA
NG_061543.1:g.11516_11517insCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.*272_*273insCAA MANE Select	ENSP00000342007.4:n.*272_*273insCAA
ENST00000343932.4:c.*272_*273insCAA	ENSP00000342007.4:n.*272_*273insCAA
NM_000761.4:c.*272_*273insCAA	NP_000752.2:n.*272_*273insCAA
NM_000761.5:c.*272_*273insCAA MANE Select	NP_000752.2:n.*272_*273insCAA