Canonical Allele Identifier: CA2187826946
Gene: CYP1A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754606_74754615delinsAAAAAAAAAG , CM000677.2:g.74754606_74754615delinsAAAAAAAAAG GRCh38
NC_000015.9:g.75046947_75046956delinsAAAAAAAAAG , CM000677.1:g.75046947_75046956delinsAAAAAAAAAG GRCh37
NC_000015.8:g.72834000_72834009delinsAAAAAAAAAG NCBI36
NG_008431.1:g.37065_37074delinsAAAAAAAAAG
NG_008431.2:g.37065_37074delinsAAAAAAAAAG
NG_061543.1:g.10762_10771delinsAAAAAAAAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.1254-185_1254-176delinsAAAAAAAAAG MANE Select ENSP00000342007.4:n.1254-185_1254-176delinsAAAAAAAAAG
ENST00000343932.4:c.1254-185_1254-176delinsAAAAAAAAAG ENSP00000342007.4:n.1254-185_1254-176delinsAAAAAAAAAG
NM_000761.4:c.1254-185_1254-176delinsAAAAAAAAAG NP_000752.2:n.1254-185_1254-176delinsAAAAAAAAAG
NM_000761.5:c.1254-185_1254-176delinsAAAAAAAAAG MANE Select NP_000752.2:n.1254-185_1254-176delinsAAAAAAAAAG
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