Canonical Allele Identifier: CA2187826947
Gene: CYP1A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754611_74754615delinsAAAAG , CM000677.2:g.74754611_74754615delinsAAAAG GRCh38
NC_000015.9:g.75046952_75046956delinsAAAAG , CM000677.1:g.75046952_75046956delinsAAAAG GRCh37
NC_000015.8:g.72834005_72834009delinsAAAAG NCBI36
NG_008431.1:g.37070_37074delinsAAAAG
NG_008431.2:g.37070_37074delinsAAAAG
NG_061543.1:g.10767_10771delinsAAAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.1254-180_1254-176delinsAAAAG MANE Select ENSP00000342007.4:n.1254-180_1254-176delinsAAAAG
ENST00000343932.4:c.1254-180_1254-176delinsAAAAG ENSP00000342007.4:n.1254-180_1254-176delinsAAAAG
NM_000761.4:c.1254-180_1254-176delinsAAAAG NP_000752.2:n.1254-180_1254-176delinsAAAAG
NM_000761.5:c.1254-180_1254-176delinsAAAAG MANE Select NP_000752.2:n.1254-180_1254-176delinsAAAAG
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