Canonical Allele Identifier: CA1108695649
Gene: AOC1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150832330_150832331insTTTTTTTTTT , CM000669.2:g.150832330_150832331insTTTTTTTTTT GRCh38
NC_000007.13:g.150529418_150529419insTTTTTTTTTT , CM000669.1:g.150529418_150529419insTTTTTTTTTT GRCh37
NC_000007.12:g.150160351_150160352insTTTTTTTTTT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000467291.5:c.-93+4928_-93+4929insTTTTTTTTTT ENSP00000418328.1:n.-93+4928_-93+4929insTTTTTTTTTT
ENST00000493429.5:c.-93+4928_-93+4929insTTTTTTTTTT ENSP00000418614.1:n.-93+4928_-93+4929insTTTTTTTTTT
XM_011516008.1:c.-182+4928_-182+4929insTTTTTTTTTT XP_011514310.1:n.-182+4928_-182+4929insTTTTTTTTTT
XR_928169.1:n.352-3422_352-3421insAAAAAAAAAA
XR_928170.1:n.482-3422_482-3421insAAAAAAAAAA
XR_928171.1:n.354-3422_354-3421insAAAAAAAAAA
XM_017011944.1:c.-93+4928_-93+4929insTTTTTTTTTT XP_016867433.1:n.-93+4928_-93+4929insTTTTTTTTTT
XM_017011945.1:c.-93+4928_-93+4929insTTTTTTTTTT XP_016867434.1:n.-93+4928_-93+4929insTTTTTTTTTT
XR_928169.2:n.358-3422_358-3421insAAAAAAAAAA
XR_928171.2:n.358-3422_358-3421insAAAAAAAAAA
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