Canonical Allele Identifier: CA336129012

Gene: MAGEC3

Linked Data

• dbSNP Id: rs761811031
• gnomAD v3: X-141895212-T-TG
• gnomAD v4: X-141895212-T-TG
• MyVariant Identifiers: chrX:g.140982998_140982999insG (hg19) ; chrX:g.141895212_141895213insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.141895218dup , CM000685.2:g.141895218dup	GRCh38
NC_000023.10:g.140983004dup , CM000685.1:g.140983004dup	GRCh37
NC_000023.9:g.140810670dup	NCBI36
NG_013272.1:g.61903dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298296.1:c.910-51dup MANE Select	ENSP00000298296.1:n.910-51dup
ENST00000443323.2:c.-118-1213dup	ENSP00000438254.1:n.-118-1213dup
ENST00000483584.5:n.150-51dup
ENST00000544766.5:c.-378-51dup	ENSP00000440444.1:n.-378-51dup
NM_138702.1:c.910-51dup MANE Select	NP_619647.1:n.910-51dup
NM_177456.2:c.-378-51dup	NP_803251.1:n.-378-51dup
XM_011531267.1:c.-352dup	XP_011529569.1:n.-352dup
XM_011531267.3:c.-352dup	XP_011529569.1:n.-352dup
XM_017029265.2:c.-378-51dup	XP_016884754.1:n.-378-51dup