Canonical Allele Identifier: CA1752388512
Gene: AOC1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150861307T= , CM000669.2:g.150861307T= GRCh38
NC_000007.13:g.150558395T= , CM000669.1:g.150558395T= GRCh37
NC_000007.12:g.150189328T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000360937.9:c.*98T= MANE Select ENSP00000354193.4:n.*98T=
ENST00000360937.8:c.*98T= ENSP00000354193.4:n.*98T=
ENST00000467291.5:c.*98T= ENSP00000418328.1:n.*98T=
ENST00000493429.5:c.*98T= ENSP00000418614.1:n.*98T=
XR_928169.1:n.295+15702A=
XR_928170.1:n.425+7309A=
XR_928171.1:n.297+15702A=
XR_928169.2:n.301+15702A=
XR_928171.2:n.301+15702A=
NM_001091.4:c.*98T= MANE Select NP_001082.2:n.*98T=
NM_001272072.2:c.*98T= NP_001259001.1:n.*98T=
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