Canonical Allele Identifier: CA2629509347
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74751907_74751908insGAACCAGAAC , CM000677.2:g.74751907_74751908insGAACCAGAAC GRCh38
NC_000015.9:g.75044248_75044249insGAACCAGAAC , CM000677.1:g.75044248_75044249insGAACCAGAAC GRCh37
NC_000015.8:g.72831301_72831302insGAACCAGAAC NCBI36
NG_008431.1:g.34366_34367insGAACCAGAAC
NG_008431.2:g.34366_34367insGAACCAGAAC
NG_061543.1:g.8063_8064insGAACCAGAAC

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1042+53_1042+54insGAACCAGAAC MANE Select ENSP00000342007.4:n.1042+53_1042+54insGAA...
ENST00000343932.4:c.1042+53_1042+54insGAACCAGAAC ENSP00000342007.4:n.1042+53_1042+54insGAA...
NM_000761.4:c.1042+53_1042+54insGAACCAGAAC NP_000752.2:n.1042+53_1042+54insGAACCAGAA...
NM_000761.5:c.1042+53_1042+54insGAACCAGAAC MANE Select NP_000752.2:n.1042+53_1042+54insGAACCAGAA...