Canonical Allele Identifier: CA414436733
Gene: MAGEC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.140983167G>C (hg19) chrX:g.141895381G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.141895381G>C , CM000685.2:g.141895381G>C GRCh38
NC_000023.10:g.140983167G>C , CM000685.1:g.140983167G>C GRCh37
NC_000023.9:g.140810833G>C NCBI36
NG_013272.1:g.62066G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000298296.1:c.1022G>C MANE Select ENSP00000298296.1:p.Ser341Thr
ENST00000443323.2:c.-118-1050G>C ENSP00000438254.1:n.-118-1050G>C
ENST00000483584.5:n.262G>C
ENST00000544766.5:c.-266G>C ENSP00000440444.1:n.-266G>C
NM_138702.1:c.1022G>C MANE Select NP_619647.1:p.Ser341Thr
NM_177456.2:c.-266G>C NP_803251.1:n.-266G>C
XM_011531267.1:c.-189G>C XP_011529569.1:n.-189G>C
XM_011531267.3:c.-189G>C XP_011529569.1:n.-189G>C
XM_017029265.2:c.-266G>C XP_016884754.1:n.-266G>C
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