Canonical Allele Identifier: CA414436759
Gene: MAGEC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.140983172T>G (hg19) chrX:g.141895386T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.141895386T>G , CM000685.2:g.141895386T>G GRCh38
NC_000023.10:g.140983172T>G , CM000685.1:g.140983172T>G GRCh37
NC_000023.9:g.140810838T>G NCBI36
NG_013272.1:g.62071T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000298296.1:c.1027T>G MANE Select ENSP00000298296.1:p.Leu343Val
ENST00000443323.2:c.-118-1045T>G ENSP00000438254.1:n.-118-1045T>G
ENST00000483584.5:n.267T>G
ENST00000544766.5:c.-261T>G ENSP00000440444.1:n.-261T>G
NM_138702.1:c.1027T>G MANE Select NP_619647.1:p.Leu343Val
NM_177456.2:c.-261T>G NP_803251.1:n.-261T>G
XM_011531267.1:c.-184T>G XP_011529569.1:n.-184T>G
XM_011531267.3:c.-184T>G XP_011529569.1:n.-184T>G
XM_017029265.2:c.-261T>G XP_016884754.1:n.-261T>G
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