Canonical Allele Identifier: CA2187827260
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755276_74755286delinsCCAACATAGTG , CM000677.2:g.74755276_74755286delinsCCAACATAGTG GRCh38
NC_000015.9:g.75047617_75047627delinsCCAACATAGTG , CM000677.1:g.75047617_75047627delinsCCAACATAGTG GRCh37
NC_000015.8:g.72834670_72834680delinsCCAACATAGTG NCBI36
NG_008431.1:g.37735_37745delinsCCAACATAGTG
NG_008431.2:g.37735_37745delinsCCAACATAGTG
NG_061543.1:g.11432_11442delinsCCAACATAGTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*188_*198delinsCCAACATAGTG MANE Select ENSP00000342007.4:n.*188_*198delinsCCAACATAGTG
ENST00000343932.4:c.*188_*198delinsCCAACATAGTG ENSP00000342007.4:n.*188_*198delinsCCAACATAGTG
NM_000761.4:c.*188_*198delinsCCAACATAGTG NP_000752.2:n.*188_*198delinsCCAACATAGTG
NM_000761.5:c.*188_*198delinsCCAACATAGTG MANE Select NP_000752.2:n.*188_*198delinsCCAACATAGTG