Canonical Allele Identifier: CA971501077
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755350_74755351insCA , CM000677.2:g.74755350_74755351insCA GRCh38
NC_000015.9:g.75047691_75047692insCA , CM000677.1:g.75047691_75047692insCA GRCh37
NC_000015.8:g.72834744_72834745insCA NCBI36
NG_008431.1:g.37809_37810insCA
NG_008431.2:g.37809_37810insCA
NG_061543.1:g.11506_11507insCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*262_*263insCA MANE Select ENSP00000342007.4:n.*262_*263insCA
ENST00000343932.4:c.*262_*263insCA ENSP00000342007.4:n.*262_*263insCA
NM_000761.4:c.*262_*263insCA NP_000752.2:n.*262_*263insCA
NM_000761.5:c.*262_*263insCA MANE Select NP_000752.2:n.*262_*263insCA