Canonical Allele Identifier: CA414436791
Gene: MAGEC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.140983177C>G (hg19) chrX:g.141895391C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.141895391C>G , CM000685.2:g.141895391C>G GRCh38
NC_000023.10:g.140983177C>G , CM000685.1:g.140983177C>G GRCh37
NC_000023.9:g.140810843C>G NCBI36
NG_013272.1:g.62076C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000298296.1:c.1032C>G MANE Select ENSP00000298296.1:p.Asp344Glu
ENST00000443323.2:c.-118-1040C>G ENSP00000438254.1:n.-118-1040C>G
ENST00000483584.5:n.272C>G
ENST00000544766.5:c.-256C>G ENSP00000440444.1:n.-256C>G
NM_138702.1:c.1032C>G MANE Select NP_619647.1:p.Asp344Glu
NM_177456.2:c.-256C>G NP_803251.1:n.-256C>G
XM_011531267.1:c.-179C>G XP_011529569.1:n.-179C>G
XM_011531267.3:c.-179C>G XP_011529569.1:n.-179C>G
XM_017029265.2:c.-256C>G XP_016884754.1:n.-256C>G
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