Canonical Allele Identifier: CA2804766387
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755356_74755361dup , CM000677.2:g.74755356_74755361dup GRCh38
NC_000015.9:g.75047697_75047702dup , CM000677.1:g.75047697_75047702dup GRCh37
NC_000015.8:g.72834750_72834755dup NCBI36
NG_008431.1:g.37815_37820dup
NG_008431.2:g.37815_37820dup
NG_061543.1:g.11512_11517dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*268_*273dup MANE Select ENSP00000342007.4:n.*268_*273dup
ENST00000343932.4:c.*268_*273dup ENSP00000342007.4:n.*268_*273dup
NM_000761.4:c.*268_*273dup NP_000752.2:n.*268_*273dup
NM_000761.5:c.*268_*273dup MANE Select NP_000752.2:n.*268_*273dup