Canonical Allele Identifier: CA2187827316
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755362_74755363delinsCA , CM000677.2:g.74755362_74755363delinsCA GRCh38
NC_000015.9:g.75047703_75047704delinsCA , CM000677.1:g.75047703_75047704delinsCA GRCh37
NC_000015.8:g.72834756_72834757delinsCA NCBI36
NG_008431.1:g.37821_37822delinsCA
NG_008431.2:g.37821_37822delinsCA
NG_061543.1:g.11518_11519delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*274_*275delinsCA MANE Select ENSP00000342007.4:n.*274_*275delinsCA
ENST00000343932.4:c.*274_*275delinsCA ENSP00000342007.4:n.*274_*275delinsCA
NM_000761.4:c.*274_*275delinsCA NP_000752.2:n.*274_*275delinsCA
NM_000761.5:c.*274_*275delinsCA MANE Select NP_000752.2:n.*274_*275delinsCA