Canonical Allele Identifier: CA2187827307
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755358_74755362delinsAAAAC , CM000677.2:g.74755358_74755362delinsAAAAC GRCh38
NC_000015.9:g.75047699_75047703delinsAAAAC , CM000677.1:g.75047699_75047703delinsAAAAC GRCh37
NC_000015.8:g.72834752_72834756delinsAAAAC NCBI36
NG_008431.1:g.37817_37821delinsAAAAC
NG_008431.2:g.37817_37821delinsAAAAC
NG_061543.1:g.11514_11518delinsAAAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*270_*274delinsAAAAC MANE Select ENSP00000342007.4:n.*270_*274delinsAAAAC
ENST00000343932.4:c.*270_*274delinsAAAAC ENSP00000342007.4:n.*270_*274delinsAAAAC
NM_000761.4:c.*270_*274delinsAAAAC NP_000752.2:n.*270_*274delinsAAAAC
NM_000761.5:c.*270_*274delinsAAAAC MANE Select NP_000752.2:n.*270_*274delinsAAAAC