Canonical Allele Identifier: CA2629512231
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755376_74755380dup , CM000677.2:g.74755376_74755380dup GRCh38
NC_000015.9:g.75047717_75047721dup , CM000677.1:g.75047717_75047721dup GRCh37
NC_000015.8:g.72834770_72834774dup NCBI36
NG_008431.1:g.37835_37839dup
NG_008431.2:g.37835_37839dup
NG_061543.1:g.11532_11536dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*288_*292dup MANE Select ENSP00000342007.4:n.*288_*292dup
ENST00000343932.4:c.*288_*292dup ENSP00000342007.4:n.*288_*292dup
NM_000761.4:c.*288_*292dup NP_000752.2:n.*288_*292dup
NM_000761.5:c.*288_*292dup MANE Select NP_000752.2:n.*288_*292dup