Canonical Allele Identifier: CA413272269

Gene: MAGED2

Linked Data

• MyVariant Identifiers: chrX:g.54838612A>T (hg19) ; chrX:g.54812179A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.54812179A>T , CM000685.2:g.54812179A>T	GRCh38
NC_000023.10:g.54838612A>T , CM000685.1:g.54838612A>T	GRCh37
NC_000023.9:g.54855337A>T	NCBI36
NG_012844.1:g.9442A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375068.6:c.1013A>T MANE Select	ENSP00000364209.1:p.Glu338Val
ENST00000218439.8:c.1013A>T	ENSP00000218439.4:p.Glu338Val
ENST00000347546.8:c.959A>T	ENSP00000336962.4:p.Glu320Val
ENST00000375053.6:c.1013A>T	ENSP00000364193.2:p.Glu338Val
ENST00000375058.5:c.1013A>T	ENSP00000364198.1:p.Glu338Val
ENST00000375060.5:c.758A>T	ENSP00000364200.1:p.Glu253Val
ENST00000375068.5:c.1013A>T	ENSP00000364209.1:p.Glu338Val
ENST00000396224.1:c.1013A>T	ENSP00000379526.1:p.Glu338Val
ENST00000487463.1:n.7A>T
ENST00000487482.5:n.145A>T
ENST00000627068.2:c.758A>T	ENSP00000486563.1:p.Glu253Val
NM_014599.5:c.1013A>T	NP_055414.2:p.Glu338Val
NM_177433.2:c.1013A>T	NP_803182.1:p.Glu338Val
NM_201222.2:c.1013A>T	NP_957516.1:p.Glu338Val
NM_177433.3:c.1013A>T MANE Select	NP_803182.1:p.Glu338Val
NM_014599.6:c.1013A>T	NP_055414.2:p.Glu338Val
NM_201222.3:c.1013A>T	NP_957516.1:p.Glu338Val