Canonical Allele Identifier: CA2187827300
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755353_74755370delinsAAAAAAAAACAAACAAAC , CM000677.2:g.74755353_74755370delinsAAAAAAAAACAAACAAAC GRCh38
NC_000015.9:g.75047694_75047711delinsAAAAAAAAACAAACAAAC , CM000677.1:g.75047694_75047711delinsAAAAAAAAACAAACAAAC GRCh37
NC_000015.8:g.72834747_72834764delinsAAAAAAAAACAAACAAAC NCBI36
NG_008431.1:g.37812_37829delinsAAAAAAAAACAAACAAAC
NG_008431.2:g.37812_37829delinsAAAAAAAAACAAACAAAC
NG_061543.1:g.11509_11526delinsAAAAAAAAACAAACAAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*265_*282delinsAAAAAAAAACAAACAAAC MANE Select ENSP00000342007.4:n.*265_*282delinsAAAAAAAAACAAACAAAC
ENST00000343932.4:c.*265_*282delinsAAAAAAAAACAAACAAAC ENSP00000342007.4:n.*265_*282delinsAAAAAAAAACAAACAAAC
NM_000761.4:c.*265_*282delinsAAAAAAAAACAAACAAAC NP_000752.2:n.*265_*282delinsAAAAAAAAACAAACAAAC
NM_000761.5:c.*265_*282delinsAAAAAAAAACAAACAAAC MANE Select NP_000752.2:n.*265_*282delinsAAAAAAAAACAAACAAAC