Canonical Allele Identifier: CA2187826933
Gene: CYP1A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754566_74754568delinsACT , CM000677.2:g.74754566_74754568delinsACT GRCh38
NC_000015.9:g.75046907_75046909delinsACT , CM000677.1:g.75046907_75046909delinsACT GRCh37
NC_000015.8:g.72833960_72833962delinsACT NCBI36
NG_008431.1:g.37025_37027delinsACT
NG_008431.2:g.37025_37027delinsACT
NG_061543.1:g.10722_10724delinsACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.1254-225_1254-223delinsACT MANE Select ENSP00000342007.4:n.1254-225_1254-223delinsACT
ENST00000343932.4:c.1254-225_1254-223delinsACT ENSP00000342007.4:n.1254-225_1254-223delinsACT
NM_000761.4:c.1254-225_1254-223delinsACT NP_000752.2:n.1254-225_1254-223delinsACT
NM_000761.5:c.1254-225_1254-223delinsACT MANE Select NP_000752.2:n.1254-225_1254-223delinsACT
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