Canonical Allele Identifier: CA10532740

Gene: MAGEC3

Linked Data

• dbSNP Id: rs749922630
• ExAC: X:140983249 G / T
• gnomAD v2: X-140983249-G-T
• gnomAD v3: X-141895463-G-T
• gnomAD v4: X-141895463-G-T
• MyVariant Identifiers: chrX:g.140983249G>T (hg19) ; chrX:g.141895463G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.141895463G>T , CM000685.2:g.141895463G>T	GRCh38
NC_000023.10:g.140983249G>T , CM000685.1:g.140983249G>T	GRCh37
NC_000023.9:g.140810915G>T	NCBI36
NG_013272.1:g.62148G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298296.1:c.1049-22G>T MANE Select	ENSP00000298296.1:n.1049-22G>T
ENST00000443323.2:c.-118-968G>T	ENSP00000438254.1:n.-118-968G>T
ENST00000483584.5:n.288+56G>T
ENST00000544766.5:c.-240+56G>T	ENSP00000440444.1:n.-240+56G>T
NM_138702.1:c.1049-22G>T MANE Select	NP_619647.1:n.1049-22G>T
NM_177456.2:c.-240+56G>T	NP_803251.1:n.-240+56G>T
XM_011531267.1:c.-163+56G>T	XP_011529569.1:n.-163+56G>T
XM_011531267.3:c.-163+56G>T	XP_011529569.1:n.-163+56G>T
XM_017029265.2:c.-240+56G>T	XP_016884754.1:n.-240+56G>T