Canonical Allele Identifier: CA414436770
Gene: MAGEC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.140983175G>A (hg19) chrX:g.141895389G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.141895389G>A , CM000685.2:g.141895389G>A GRCh38
NC_000023.10:g.140983175G>A , CM000685.1:g.140983175G>A GRCh37
NC_000023.9:g.140810841G>A NCBI36
NG_013272.1:g.62074G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000298296.1:c.1030G>A MANE Select ENSP00000298296.1:p.Asp344Asn
ENST00000443323.2:c.-118-1042G>A ENSP00000438254.1:n.-118-1042G>A
ENST00000483584.5:n.270G>A
ENST00000544766.5:c.-258G>A ENSP00000440444.1:n.-258G>A
NM_138702.1:c.1030G>A MANE Select NP_619647.1:p.Asp344Asn
NM_177456.2:c.-258G>A NP_803251.1:n.-258G>A
XM_011531267.1:c.-181G>A XP_011529569.1:n.-181G>A
XM_011531267.3:c.-181G>A XP_011529569.1:n.-181G>A
XM_017029265.2:c.-258G>A XP_016884754.1:n.-258G>A
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