Canonical Allele Identifier: CA2804766379
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755300_74755301insAAAA , CM000677.2:g.74755300_74755301insAAAA GRCh38
NC_000015.9:g.75047641_75047642insAAAA , CM000677.1:g.75047641_75047642insAAAA GRCh37
NC_000015.8:g.72834694_72834695insAAAA NCBI36
NG_008431.1:g.37759_37760insAAAA
NG_008431.2:g.37759_37760insAAAA
NG_061543.1:g.11456_11457insAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*212_*213insAAAA MANE Select ENSP00000342007.4:n.*212_*213insAAAA
ENST00000343932.4:c.*212_*213insAAAA ENSP00000342007.4:n.*212_*213insAAAA
NM_000761.4:c.*212_*213insAAAA NP_000752.2:n.*212_*213insAAAA
NM_000761.5:c.*212_*213insAAAA MANE Select NP_000752.2:n.*212_*213insAAAA