Canonical Allele Identifier: CA2187827325
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755366_74755367delinsCA , CM000677.2:g.74755366_74755367delinsCA GRCh38
NC_000015.9:g.75047707_75047708delinsCA , CM000677.1:g.75047707_75047708delinsCA GRCh37
NC_000015.8:g.72834760_72834761delinsCA NCBI36
NG_008431.1:g.37825_37826delinsCA
NG_008431.2:g.37825_37826delinsCA
NG_061543.1:g.11522_11523delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*278_*279delinsCA MANE Select ENSP00000342007.4:n.*278_*279delinsCA
ENST00000343932.4:c.*278_*279delinsCA ENSP00000342007.4:n.*278_*279delinsCA
NM_000761.4:c.*278_*279delinsCA NP_000752.2:n.*278_*279delinsCA
NM_000761.5:c.*278_*279delinsCA MANE Select NP_000752.2:n.*278_*279delinsCA