Canonical Allele Identifier: CA2629512136
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755301_74755302del , CM000677.2:g.74755301_74755302del GRCh38
NC_000015.9:g.75047642_75047643del , CM000677.1:g.75047642_75047643del GRCh37
NC_000015.8:g.72834695_72834696del NCBI36
NG_008431.1:g.37760_37761del
NG_008431.2:g.37760_37761del
NG_061543.1:g.11457_11458del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*213_*214del MANE Select ENSP00000342007.4:n.*213_*214del
ENST00000343932.4:c.*213_*214del ENSP00000342007.4:n.*213_*214del
NM_000761.4:c.*213_*214del NP_000752.2:n.*213_*214del
NM_000761.5:c.*213_*214del MANE Select NP_000752.2:n.*213_*214del