Canonical Allele Identifier: CA2507797798
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755241_74755244dup , CM000677.2:g.74755241_74755244dup GRCh38
NC_000015.9:g.75047582_75047585dup , CM000677.1:g.75047582_75047585dup GRCh37
NC_000015.8:g.72834635_72834638dup NCBI36
NG_008431.1:g.37700_37703dup
NG_008431.2:g.37700_37703dup
NG_061543.1:g.11397_11400dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*153_*156dup MANE Select ENSP00000342007.4:n.*153_*156dup
ENST00000343932.4:c.*153_*156dup ENSP00000342007.4:n.*153_*156dup
NM_000761.4:c.*153_*156dup NP_000752.2:n.*153_*156dup
NM_000761.5:c.*153_*156dup MANE Select NP_000752.2:n.*153_*156dup