Canonical Allele Identifier: CA872279190
Gene: MAGEC3 HGNC NCBI

Linked Data

dbSNP Id: rs760378956
gnomAD v4: X-141895136-C-CG
MyVariant Identifiers: chrX:g.140982922_140982923insG (hg19) chrX:g.141895136_141895137insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.141895142dup , CM000685.2:g.141895142dup GRCh38
NC_000023.10:g.140982928dup , CM000685.1:g.140982928dup GRCh37
NC_000023.9:g.140810594dup NCBI36
NG_013272.1:g.61827dup

Transcript Alleles

HGVS Amino-acid change
ENST00000298296.1:c.910-127dup MANE Select ENSP00000298296.1:n.910-127dup
ENST00000443323.2:c.-118-1289dup ENSP00000438254.1:n.-118-1289dup
ENST00000483584.5:n.150-127dup
ENST00000544766.5:c.-378-127dup ENSP00000440444.1:n.-378-127dup
NM_138702.1:c.910-127dup MANE Select NP_619647.1:n.910-127dup
NM_177456.2:c.-378-127dup NP_803251.1:n.-378-127dup
XM_017029265.2:c.-378-127dup XP_016884754.1:n.-378-127dup
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