Canonical Allele Identifier: CA2187827312
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755360_74755362delinsAAC , CM000677.2:g.74755360_74755362delinsAAC GRCh38
NC_000015.9:g.75047701_75047703delinsAAC , CM000677.1:g.75047701_75047703delinsAAC GRCh37
NC_000015.8:g.72834754_72834756delinsAAC NCBI36
NG_008431.1:g.37819_37821delinsAAC
NG_008431.2:g.37819_37821delinsAAC
NG_061543.1:g.11516_11518delinsAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*272_*274delinsAAC MANE Select ENSP00000342007.4:n.*272_*274delinsAAC
ENST00000343932.4:c.*272_*274delinsAAC ENSP00000342007.4:n.*272_*274delinsAAC
NM_000761.4:c.*272_*274delinsAAC NP_000752.2:n.*272_*274delinsAAC
NM_000761.5:c.*272_*274delinsAAC MANE Select NP_000752.2:n.*272_*274delinsAAC