Canonical Allele Identifier: CA10532731

Gene: MAGEC3

Linked Data

• dbSNP Id: rs759758714
• ExAC: X:140983214 C / T
• gnomAD v2: X-140983214-C-T
• gnomAD v3: X-141895428-C-T
• gnomAD v4: X-141895428-C-T
• MyVariant Identifiers: chrX:g.140983214C>T (hg19) ; chrX:g.141895428C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.141895428C>T , CM000685.2:g.141895428C>T	GRCh38
NC_000023.10:g.140983214C>T , CM000685.1:g.140983214C>T	GRCh37
NC_000023.9:g.140810880C>T	NCBI36
NG_013272.1:g.62113C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298296.1:c.1048+21C>T MANE Select	ENSP00000298296.1:n.1048+21C>T
ENST00000443323.2:c.-118-1003C>T	ENSP00000438254.1:n.-118-1003C>T
ENST00000483584.5:n.288+21C>T
ENST00000544766.5:c.-240+21C>T	ENSP00000440444.1:n.-240+21C>T
NM_138702.1:c.1048+21C>T MANE Select	NP_619647.1:n.1048+21C>T
NM_177456.2:c.-240+21C>T	NP_803251.1:n.-240+21C>T
XM_011531267.1:c.-163+21C>T	XP_011529569.1:n.-163+21C>T
XM_011531267.3:c.-163+21C>T	XP_011529569.1:n.-163+21C>T
XM_017029265.2:c.-240+21C>T	XP_016884754.1:n.-240+21C>T