Canonical Allele Identifier: CA516581022

Gene: MAGED2

Linked Data

• MyVariant Identifiers: chrX:g.54838598G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.54812165G>C , CM000685.2:g.54812165G>C	GRCh38
NC_000023.10:g.54838598G>C , CM000685.1:g.54838598G>C	GRCh37
NC_000023.9:g.54855323G>C	NCBI36
NG_012844.1:g.9428G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000375068.6:c.999G>C MANE Select	ENSP00000364209.1:p.Gly333=
ENST00000218439.8:c.999G>C	ENSP00000218439.4:p.Gly333=
ENST00000347546.8:c.945G>C	ENSP00000336962.4:p.Gly315=
ENST00000375053.6:c.999G>C	ENSP00000364193.2:p.Gly333=
ENST00000375058.5:c.999G>C	ENSP00000364198.1:p.Gly333=
ENST00000375060.5:c.744G>C	ENSP00000364200.1:p.Gly248=
ENST00000375068.5:c.999G>C	ENSP00000364209.1:p.Gly333=
ENST00000396224.1:c.999G>C	ENSP00000379526.1:p.Gly333=
ENST00000487482.5:n.131G>C
ENST00000627068.2:c.744G>C	ENSP00000486563.1:p.Gly248=
NM_014599.5:c.999G>C	NP_055414.2:p.Gly333=
NM_177433.2:c.999G>C	NP_803182.1:p.Gly333=
NM_201222.2:c.999G>C	NP_957516.1:p.Gly333=
NM_177433.3:c.999G>C MANE Select	NP_803182.1:p.Gly333=
NM_014599.6:c.999G>C	NP_055414.2:p.Gly333=
NM_201222.3:c.999G>C	NP_957516.1:p.Gly333=