Canonical Allele Identifier: CA414435658
Gene: MAGEC3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2246542
ClinVar RCV Id: RCV004104467

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.141895269C>A , CM000685.2:g.141895269C>A GRCh38
NC_000023.10:g.140983055C>A , CM000685.1:g.140983055C>A GRCh37
NC_000023.9:g.140810721C>A NCBI36
NG_013272.1:g.61954C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000298296.1:c.910C>A MANE Select ENSP00000298296.1:p.Pro304Thr
ENST00000443323.2:c.-118-1162C>A ENSP00000438254.1:n.-118-1162C>A
ENST00000483584.5:n.150C>A
ENST00000544766.5:c.-378C>A ENSP00000440444.1:n.-378C>A
NM_138702.1:c.910C>A MANE Select NP_619647.1:p.Pro304Thr
NM_177456.2:c.-378C>A NP_803251.1:n.-378C>A
XM_011531267.1:c.-301C>A XP_011529569.1:n.-301C>A
XM_011531267.3:c.-301C>A XP_011529569.1:n.-301C>A
XM_017029265.2:c.-378C>A XP_016884754.1:n.-378C>A