Canonical Allele Identifier: CA2187826268
Gene: CYP1A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74753232_74753234delinsCTG , CM000677.2:g.74753232_74753234delinsCTG GRCh38
NC_000015.9:g.75045573_75045575delinsCTG , CM000677.1:g.75045573_75045575delinsCTG GRCh37
NC_000015.8:g.72832626_72832628delinsCTG NCBI36
NG_008431.1:g.35691_35693delinsCTG
NG_008431.2:g.35691_35693delinsCTG
NG_061543.1:g.9388_9390delinsCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.1215_1217delinsCTG MANE Select ENSP00000342007.4:p.Cys405=
ENST00000343932.4:c.1215_1217delinsCTG ENSP00000342007.4:p.Cys405=
NM_000761.4:c.1215_1217delinsCTG NP_000752.2:p.Cys405=
NM_000761.5:c.1215_1217delinsCTG MANE Select NP_000752.2:p.Cys405=
Search 100 bp 5'
Search 100 bp 3'