Canonical Allele Identifier: CA10532766

Gene: MAGEC3

Linked Data

• dbSNP Id: rs746706209
• ExAC: X:140983364 A / G
• gnomAD v2: X-140983364-A-G
• gnomAD v3: X-141895578-A-G
• gnomAD v4: X-141895578-A-G
• MyVariant Identifiers: chrX:g.140983364A>G (hg19) ; chrX:g.141895578A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.141895578A>G , CM000685.2:g.141895578A>G	GRCh38
NC_000023.10:g.140983364A>G , CM000685.1:g.140983364A>G	GRCh37
NC_000023.9:g.140811030A>G	NCBI36
NG_013272.1:g.62263A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298296.1:c.1123+19A>G MANE Select	ENSP00000298296.1:n.1123+19A>G
ENST00000443323.2:c.-118-853A>G	ENSP00000438254.1:n.-118-853A>G
ENST00000483584.5:n.288+171A>G
ENST00000544766.5:c.-240+171A>G	ENSP00000440444.1:n.-240+171A>G
NM_138702.1:c.1123+19A>G MANE Select	NP_619647.1:n.1123+19A>G
NM_177456.2:c.-240+171A>G	NP_803251.1:n.-240+171A>G
XM_011531267.1:c.-163+171A>G	XP_011529569.1:n.-163+171A>G
XM_011531267.3:c.-163+171A>G	XP_011529569.1:n.-163+171A>G
XM_017029265.2:c.-240+171A>G	XP_016884754.1:n.-240+171A>G