Canonical Allele Identifier: CA2804766391
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755371_74755372insGA , CM000677.2:g.74755371_74755372insGA GRCh38
NC_000015.9:g.75047712_75047713insGA , CM000677.1:g.75047712_75047713insGA GRCh37
NC_000015.8:g.72834765_72834766insGA NCBI36
NG_008431.1:g.37830_37831insGA
NG_008431.2:g.37830_37831insGA
NG_061543.1:g.11527_11528insGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*283_*284insGA MANE Select ENSP00000342007.4:n.*283_*284insGA
ENST00000343932.4:c.*283_*284insGA ENSP00000342007.4:n.*283_*284insGA
NM_000761.4:c.*283_*284insGA NP_000752.2:n.*283_*284insGA
NM_000761.5:c.*283_*284insGA MANE Select NP_000752.2:n.*283_*284insGA