Canonical Allele Identifier: CA414437316

Gene: MAGEC3

Linked Data

• MyVariant Identifiers: chrX:g.140983343G>T (hg19) ; chrX:g.141895557G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.141895557G>T , CM000685.2:g.141895557G>T	GRCh38
NC_000023.10:g.140983343G>T , CM000685.1:g.140983343G>T	GRCh37
NC_000023.9:g.140811009G>T	NCBI36
NG_013272.1:g.62242G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298296.1:c.1121G>T MANE Select	ENSP00000298296.1:p.Gly374Val
ENST00000443323.2:c.-118-874G>T	ENSP00000438254.1:n.-118-874G>T
ENST00000483584.5:n.288+150G>T
ENST00000544766.5:c.-240+150G>T	ENSP00000440444.1:n.-240+150G>T
NM_138702.1:c.1121G>T MANE Select	NP_619647.1:p.Gly374Val
NM_177456.2:c.-240+150G>T	NP_803251.1:n.-240+150G>T
XM_011531267.1:c.-163+150G>T	XP_011529569.1:n.-163+150G>T
XM_011531267.3:c.-163+150G>T	XP_011529569.1:n.-163+150G>T
XM_017029265.2:c.-240+150G>T	XP_016884754.1:n.-240+150G>T