Canonical Allele Identifier: CA2514030226
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749939del , CM000677.2:g.74749939del GRCh38
NC_000015.9:g.75042280del , CM000677.1:g.75042280del GRCh37
NC_000015.8:g.72829333del NCBI36
NG_008431.1:g.32398del
NG_008431.2:g.32398del
NG_061543.1:g.6095del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.201del MANE Select ENSP00000342007.4:p.Met68Ter
ENST00000343932.4:c.201del ENSP00000342007.4:p.Met68Ter
NM_000761.4:c.201del NP_000752.2:p.Met68Ter
NM_000761.5:c.201del MANE Select NP_000752.2:p.Met68Ter