Canonical Allele Identifier: CA414437166

Gene: MAGEC3

Linked Data

• MyVariant Identifiers: chrX:g.140983318G>A (hg19) ; chrX:g.141895532G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.141895532G>A , CM000685.2:g.141895532G>A	GRCh38
NC_000023.10:g.140983318G>A , CM000685.1:g.140983318G>A	GRCh37
NC_000023.9:g.140810984G>A	NCBI36
NG_013272.1:g.62217G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298296.1:c.1096G>A MANE Select	ENSP00000298296.1:p.Ala366Thr
ENST00000443323.2:c.-118-899G>A	ENSP00000438254.1:n.-118-899G>A
ENST00000483584.5:n.288+125G>A
ENST00000544766.5:c.-240+125G>A	ENSP00000440444.1:n.-240+125G>A
NM_138702.1:c.1096G>A MANE Select	NP_619647.1:p.Ala366Thr
NM_177456.2:c.-240+125G>A	NP_803251.1:n.-240+125G>A
XM_011531267.1:c.-163+125G>A	XP_011529569.1:n.-163+125G>A
XM_011531267.3:c.-163+125G>A	XP_011529569.1:n.-163+125G>A
XM_017029265.2:c.-240+125G>A	XP_016884754.1:n.-240+125G>A