Canonical Allele Identifier: CA2629512238
Gene: CYP1A2 HGNC NCBI

Linked Data

gnomAD v4: 15-74755380-A-AAAC
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755380_74755381insAAC , CM000677.2:g.74755380_74755381insAAC GRCh38
NC_000015.9:g.75047721_75047722insAAC , CM000677.1:g.75047721_75047722insAAC GRCh37
NC_000015.8:g.72834774_72834775insAAC NCBI36
NG_008431.1:g.37839_37840insAAC
NG_008431.2:g.37839_37840insAAC
NG_061543.1:g.11536_11537insAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*292_*293insAAC MANE Select ENSP00000342007.4:n.*292_*293insAAC
ENST00000343932.4:c.*292_*293insAAC ENSP00000342007.4:n.*292_*293insAAC
NM_000761.4:c.*292_*293insAAC NP_000752.2:n.*292_*293insAAC
NM_000761.5:c.*292_*293insAAC MANE Select NP_000752.2:n.*292_*293insAAC
Search 100 bp 5'
Search 100 bp 3'