Canonical Allele Identifier: CA2187827326
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755366_74755371delinsCAAACA , CM000677.2:g.74755366_74755371delinsCAAACA GRCh38
NC_000015.9:g.75047707_75047712delinsCAAACA , CM000677.1:g.75047707_75047712delinsCAAACA GRCh37
NC_000015.8:g.72834760_72834765delinsCAAACA NCBI36
NG_008431.1:g.37825_37830delinsCAAACA
NG_008431.2:g.37825_37830delinsCAAACA
NG_061543.1:g.11522_11527delinsCAAACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*278_*283delinsCAAACA MANE Select ENSP00000342007.4:n.*278_*283delinsCAAACA
ENST00000343932.4:c.*278_*283delinsCAAACA ENSP00000342007.4:n.*278_*283delinsCAAACA
NM_000761.4:c.*278_*283delinsCAAACA NP_000752.2:n.*278_*283delinsCAAACA
NM_000761.5:c.*278_*283delinsCAAACA MANE Select NP_000752.2:n.*278_*283delinsCAAACA