Canonical Allele Identifier: CA518858387
Gene: MAGEC3 HGNC NCBI

Linked Data

gnomAD v4: X-141895388-A-G
MyVariant Identifiers: chrX:g.140983174A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.141895388A>G , CM000685.2:g.141895388A>G GRCh38
NC_000023.10:g.140983174A>G , CM000685.1:g.140983174A>G GRCh37
NC_000023.9:g.140810840A>G NCBI36
NG_013272.1:g.62073A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000298296.1:c.1029A>G MANE Select ENSP00000298296.1:p.Leu343=
ENST00000443323.2:c.-118-1043A>G ENSP00000438254.1:n.-118-1043A>G
ENST00000483584.5:n.269A>G
ENST00000544766.5:c.-259A>G ENSP00000440444.1:n.-259A>G
NM_138702.1:c.1029A>G MANE Select NP_619647.1:p.Leu343=
NM_177456.2:c.-259A>G NP_803251.1:n.-259A>G
XM_011531267.1:c.-182A>G XP_011529569.1:n.-182A>G
XM_011531267.3:c.-182A>G XP_011529569.1:n.-182A>G
XM_017029265.2:c.-259A>G XP_016884754.1:n.-259A>G
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