Canonical Allele Identifier: CA413265628

Gene: MAGED2

Linked Data

• MyVariant Identifiers: chrX:g.54836395G>A (hg19) ; chrX:g.54809962G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.54809962G>A , CM000685.2:g.54809962G>A	GRCh38
NC_000023.10:g.54836395G>A , CM000685.1:g.54836395G>A	GRCh37
NC_000023.9:g.54853120G>A	NCBI36
NG_012844.1:g.7225G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000375068.6:c.286G>A MANE Select	ENSP00000364209.1:p.Ala96Thr
ENST00000218439.8:c.286G>A	ENSP00000218439.4:p.Ala96Thr
ENST00000347546.8:c.232G>A	ENSP00000336962.4:p.Ala78Thr
ENST00000375053.6:c.286G>A	ENSP00000364193.2:p.Ala96Thr
ENST00000375058.5:c.286G>A	ENSP00000364198.1:p.Ala96Thr
ENST00000375060.5:c.172G>A	ENSP00000364200.1:p.Ala58Thr
ENST00000375068.5:c.286G>A	ENSP00000364209.1:p.Ala96Thr
ENST00000396224.1:c.286G>A	ENSP00000379526.1:p.Ala96Thr
ENST00000463787.5:n.123-156G>A
ENST00000485483.1:n.521G>A
ENST00000497484.1:n.429G>A
ENST00000627068.2:c.172G>A	ENSP00000486563.1:p.Ala58Thr
NM_014599.5:c.286G>A	NP_055414.2:p.Ala96Thr
NM_177433.2:c.286G>A	NP_803182.1:p.Ala96Thr
NM_201222.2:c.286G>A	NP_957516.1:p.Ala96Thr
NM_177433.3:c.286G>A MANE Select	NP_803182.1:p.Ala96Thr
NM_014599.6:c.286G>A	NP_055414.2:p.Ala96Thr
NM_201222.3:c.286G>A	NP_957516.1:p.Ala96Thr