Canonical Allele Identifier: CA1137910913
Gene: MAGEC3 HGNC NCBI

Linked Data

gnomAD v3: X-141894934-TGGGAGGTGGGTAGGAAAAGGTGGGAGGGAGTGGGAAAGTGGGCAGGAAGGAGTGGGAGTGGTGGGAATATGGGCAATAAAAGGTGAAAGGGGGCAGTAGGTGAACAGGAAAGGGTGGGAAGGGGCG-T
gnomAD v4: X-141894934-TGGGAGGTGGGTAGGAAAAGGTGGGAGGGAGTGGGAAAGTGGGCAGGAAGGAGTGGGAGTGGTGGGAATATGGGCAATAAAAGGTGAAAGGGGGCAGTAGGTGAACAGGAAAGGGTGGGAAGGGGCG-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.141894945_141895070del , CM000685.2:g.141894945_141895070del GRCh38
NC_000023.10:g.140982731_140982856del , CM000685.1:g.140982731_140982856del GRCh37
NC_000023.9:g.140810397_140810522del NCBI36
NG_013272.1:g.61630_61755del

Transcript Alleles

HGVS Amino-acid Change
ENST00000298296.1:c.910-324_910-199del MANE Select ENSP00000298296.1:n.910-324_910-199del
ENST00000443323.2:c.-118-1486_-118-1361del ENSP00000438254.1:n.-118-1486_-118-1361del
ENST00000483584.5:n.149+131_150-199del
ENST00000544766.5:c.-379+131_-378-199del ENSP00000440444.1:n.-379+131_-378-199del
NM_138702.1:c.910-324_910-199del MANE Select NP_619647.1:n.910-324_910-199del
NM_177456.2:c.-379+131_-378-199del NP_803251.1:n.-379+131_-378-199del
XM_017029265.2:c.-379+131_-378-199del XP_016884754.1:n.-379+131_-378-199del
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