Canonical Allele Identifier: CA2187827330
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755369_74755370delinsAC , CM000677.2:g.74755369_74755370delinsAC GRCh38
NC_000015.9:g.75047710_75047711delinsAC , CM000677.1:g.75047710_75047711delinsAC GRCh37
NC_000015.8:g.72834763_72834764delinsAC NCBI36
NG_008431.1:g.37828_37829delinsAC
NG_008431.2:g.37828_37829delinsAC
NG_061543.1:g.11525_11526delinsAC

Transcript Alleles

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