Canonical Allele Identifier: CA336128995
Gene: MAGEC3 HGNC NCBI

Linked Data

dbSNP Id: rs760378956
gnomAD v3: X-141895136-CG-C
gnomAD v4: X-141895136-CG-C
MyVariant Identifiers: chrX:g.140982923del (hg19) chrX:g.141895137del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.141895142del , CM000685.2:g.141895142del GRCh38
NC_000023.10:g.140982928del , CM000685.1:g.140982928del GRCh37
NC_000023.9:g.140810594del NCBI36
NG_013272.1:g.61827del

Transcript Alleles

HGVS Amino-acid change
ENST00000298296.1:c.910-127del MANE Select ENSP00000298296.1:n.910-127del
ENST00000443323.2:c.-118-1289del ENSP00000438254.1:n.-118-1289del
ENST00000483584.5:n.150-127del
ENST00000544766.5:c.-378-127del ENSP00000440444.1:n.-378-127del
NM_138702.1:c.910-127del MANE Select NP_619647.1:n.910-127del
NM_177456.2:c.-378-127del NP_803251.1:n.-378-127del
XM_017029265.2:c.-378-127del XP_016884754.1:n.-378-127del
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