Canonical Allele Identifier: CA2629512226

Gene: CYP1A2

Linked Data

• gnomAD v4: 15-74755366-C-CAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74755369_74755370insAAAA , CM000677.2:g.74755369_74755370insAAAA	GRCh38
NC_000015.9:g.75047710_75047711insAAAA , CM000677.1:g.75047710_75047711insAAAA	GRCh37
NC_000015.8:g.72834763_72834764insAAAA	NCBI36
NG_008431.1:g.37828_37829insAAAA
NG_008431.2:g.37828_37829insAAAA
NG_061543.1:g.11525_11526insAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.*281_*282insAAAA MANE Select	ENSP00000342007.4:n.*281_*282insAAAA
ENST00000343932.4:c.*281_*282insAAAA	ENSP00000342007.4:n.*281_*282insAAAA
NM_000761.4:c.*281_*282insAAAA	NP_000752.2:n.*281_*282insAAAA
NM_000761.5:c.*281_*282insAAAA MANE Select	NP_000752.2:n.*281_*282insAAAA