Canonical Allele Identifier: CA2629512209
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755359_74755361del , CM000677.2:g.74755359_74755361del GRCh38
NC_000015.9:g.75047700_75047702del , CM000677.1:g.75047700_75047702del GRCh37
NC_000015.8:g.72834753_72834755del NCBI36
NG_008431.1:g.37818_37820del
NG_008431.2:g.37818_37820del
NG_061543.1:g.11515_11517del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*271_*273del MANE Select ENSP00000342007.4:n.*271_*273del
ENST00000343932.4:c.*271_*273del ENSP00000342007.4:n.*271_*273del
NM_000761.4:c.*271_*273del NP_000752.2:n.*271_*273del
NM_000761.5:c.*271_*273del MANE Select NP_000752.2:n.*271_*273del