Canonical Allele Identifier: CA518858481
Gene: MAGEC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.140983305A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.141895519A>G , CM000685.2:g.141895519A>G GRCh38
NC_000023.10:g.140983305A>G , CM000685.1:g.140983305A>G GRCh37
NC_000023.9:g.140810971A>G NCBI36
NG_013272.1:g.62204A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000298296.1:c.1083A>G MANE Select ENSP00000298296.1:p.Arg361=
ENST00000443323.2:c.-118-912A>G ENSP00000438254.1:n.-118-912A>G
ENST00000483584.5:n.288+112A>G
ENST00000544766.5:c.-240+112A>G ENSP00000440444.1:n.-240+112A>G
NM_138702.1:c.1083A>G MANE Select NP_619647.1:p.Arg361=
NM_177456.2:c.-240+112A>G NP_803251.1:n.-240+112A>G
XM_011531267.1:c.-163+112A>G XP_011529569.1:n.-163+112A>G
XM_011531267.3:c.-163+112A>G XP_011529569.1:n.-163+112A>G
XM_017029265.2:c.-240+112A>G XP_016884754.1:n.-240+112A>G