Canonical Allele Identifier: CA518858301
Gene: MAGEC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.140983135C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.141895349C>T , CM000685.2:g.141895349C>T GRCh38
NC_000023.10:g.140983135C>T , CM000685.1:g.140983135C>T GRCh37
NC_000023.9:g.140810801C>T NCBI36
NG_013272.1:g.62034C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000298296.1:c.990C>T MANE Select ENSP00000298296.1:p.Cys330=
ENST00000443323.2:c.-118-1082C>T ENSP00000438254.1:n.-118-1082C>T
ENST00000483584.5:n.230C>T
ENST00000544766.5:c.-298C>T ENSP00000440444.1:n.-298C>T
NM_138702.1:c.990C>T MANE Select NP_619647.1:p.Cys330=
NM_177456.2:c.-298C>T NP_803251.1:n.-298C>T
XM_011531267.1:c.-221C>T XP_011529569.1:n.-221C>T
XM_011531267.3:c.-221C>T XP_011529569.1:n.-221C>T
XM_017029265.2:c.-298C>T XP_016884754.1:n.-298C>T