Canonical Allele Identifier: CA414437029

Gene: MAGEC3

Linked Data

• MyVariant Identifiers: chrX:g.140983285A>T (hg19) ; chrX:g.141895499A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.141895499A>T , CM000685.2:g.141895499A>T	GRCh38
NC_000023.10:g.140983285A>T , CM000685.1:g.140983285A>T	GRCh37
NC_000023.9:g.140810951A>T	NCBI36
NG_013272.1:g.62184A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298296.1:c.1063A>T MANE Select	ENSP00000298296.1:p.Arg355Ter
ENST00000443323.2:c.-118-932A>T	ENSP00000438254.1:n.-118-932A>T
ENST00000483584.5:n.288+92A>T
ENST00000544766.5:c.-240+92A>T	ENSP00000440444.1:n.-240+92A>T
NM_138702.1:c.1063A>T MANE Select	NP_619647.1:p.Arg355Ter
NM_177456.2:c.-240+92A>T	NP_803251.1:n.-240+92A>T
XM_011531267.1:c.-163+92A>T	XP_011529569.1:n.-163+92A>T
XM_011531267.3:c.-163+92A>T	XP_011529569.1:n.-163+92A>T
XM_017029265.2:c.-240+92A>T	XP_016884754.1:n.-240+92A>T