Canonical Allele Identifier: CA2629505650
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749959_74749963del , CM000677.2:g.74749959_74749963del GRCh38
NC_000015.9:g.75042300_75042304del , CM000677.1:g.75042300_75042304del GRCh37
NC_000015.8:g.72829353_72829357del NCBI36
NG_008431.1:g.32418_32422del
NG_008431.2:g.32418_32422del
NG_061543.1:g.6115_6119del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.221_225del MANE Select ENSP00000342007.4:p.Asp74AlafsTer?
ENST00000343932.4:c.221_225del ENSP00000342007.4:p.Asp74AlafsTer?
NM_000761.4:c.221_225del NP_000752.2:p.Asp74AlafsTer?
NM_000761.5:c.221_225del MANE Select NP_000752.2:p.Asp74AlafsTer?