Canonical Allele Identifier: CA518858551

Gene: MAGEC3

Linked Data

• dbSNP Id: rs1415426282
• gnomAD v2: X-140983504-TGGGGGAGGGGTGGAGGGGA-T
• gnomAD v3: X-141895718-TGGGGGAGGGGTGGAGGGGA-T
• gnomAD v4: X-141895718-TGGGGGAGGGGTGGAGGGGA-T
• MyVariant Identifiers: chrX:g.140983505_140983523del (hg19) ; chrX:g.141895719_141895737del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.141895738_141895756del , CM000685.2:g.141895738_141895756del	GRCh38
NC_000023.10:g.140983524_140983542del , CM000685.1:g.140983524_140983542del	GRCh37
NC_000023.9:g.140811190_140811208del	NCBI36
NG_013272.1:g.62423_62441del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298296.1:c.1123+179_1123+197del MANE Select	ENSP00000298296.1:n.1123+179_1123+197del
ENST00000443323.2:c.-118-693_-118-675del	ENSP00000438254.1:n.-118-693_-118-675del
ENST00000483584.5:n.288+331_288+349del
ENST00000544766.5:c.-240+331_-240+349del	ENSP00000440444.1:n.-240+331_-240+349del
NM_138702.1:c.1123+179_1123+197del MANE Select	NP_619647.1:n.1123+179_1123+197del
NM_177456.2:c.-240+331_-240+349del	NP_803251.1:n.-240+331_-240+349del
XM_011531267.1:c.-163+331_-163+349del	XP_011529569.1:n.-163+331_-163+349del
XM_011531267.3:c.-163+331_-163+349del	XP_011529569.1:n.-163+331_-163+349del
XM_017029265.2:c.-240+331_-240+349del	XP_016884754.1:n.-240+331_-240+349del