Canonical Allele Identifier: CA10532769

Gene: MAGEC3

Linked Data

• dbSNP Id: rs180735436
• ExAC: X:140983392 G / A
• gnomAD v2: X-140983392-G-A
• gnomAD v3: X-141895606-G-A
• gnomAD v4: X-141895606-G-A
• MyVariant Identifiers: chrX:g.140983392G>A (hg19) ; chrX:g.141895606G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.141895606G>A , CM000685.2:g.141895606G>A	GRCh38
NC_000023.10:g.140983392G>A , CM000685.1:g.140983392G>A	GRCh37
NC_000023.9:g.140811058G>A	NCBI36
NG_013272.1:g.62291G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298296.1:c.1123+47G>A MANE Select	ENSP00000298296.1:n.1123+47G>A
ENST00000443323.2:c.-118-825G>A	ENSP00000438254.1:n.-118-825G>A
ENST00000483584.5:n.288+199G>A
ENST00000544766.5:c.-240+199G>A	ENSP00000440444.1:n.-240+199G>A
NM_138702.1:c.1123+47G>A MANE Select	NP_619647.1:n.1123+47G>A
NM_177456.2:c.-240+199G>A	NP_803251.1:n.-240+199G>A
XM_011531267.1:c.-163+199G>A	XP_011529569.1:n.-163+199G>A
XM_011531267.3:c.-163+199G>A	XP_011529569.1:n.-163+199G>A
XM_017029265.2:c.-240+199G>A	XP_016884754.1:n.-240+199G>A