Canonical Allele Identifier: CA2187827305
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755357_74755362delinsAAAAAC , CM000677.2:g.74755357_74755362delinsAAAAAC GRCh38
NC_000015.9:g.75047698_75047703delinsAAAAAC , CM000677.1:g.75047698_75047703delinsAAAAAC GRCh37
NC_000015.8:g.72834751_72834756delinsAAAAAC NCBI36
NG_008431.1:g.37816_37821delinsAAAAAC
NG_008431.2:g.37816_37821delinsAAAAAC
NG_061543.1:g.11513_11518delinsAAAAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*269_*274delinsAAAAAC MANE Select ENSP00000342007.4:n.*269_*274delinsAAAAAC
ENST00000343932.4:c.*269_*274delinsAAAAAC ENSP00000342007.4:n.*269_*274delinsAAAAAC
NM_000761.4:c.*269_*274delinsAAAAAC NP_000752.2:n.*269_*274delinsAAAAAC
NM_000761.5:c.*269_*274delinsAAAAAC MANE Select NP_000752.2:n.*269_*274delinsAAAAAC