Canonical Allele Identifier: CA10426706

Gene: MAGED2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.54810907C>T , CM000685.2:g.54810907C>T	GRCh38
NC_000023.10:g.54837340C>T , CM000685.1:g.54837340C>T	GRCh37
NC_000023.9:g.54854065C>T	NCBI36
NG_012844.1:g.8170C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375068.6:c.624C>T MANE Select	ENSP00000364209.1:p.Ala208=
ENST00000218439.8:c.624C>T	ENSP00000218439.4:p.Ala208=
ENST00000347546.8:c.570C>T	ENSP00000336962.4:p.Ala190=
ENST00000375053.6:c.624C>T	ENSP00000364193.2:p.Ala208=
ENST00000375058.5:c.624C>T	ENSP00000364198.1:p.Ala208=
ENST00000375060.5:c.507+3C>T	ENSP00000364200.1:n.507+3C>T
ENST00000375068.5:c.624C>T	ENSP00000364209.1:p.Ala208=
ENST00000396224.1:c.624C>T	ENSP00000379526.1:p.Ala208=
ENST00000463787.5:n.305C>T
ENST00000497484.1:n.767C>T
ENST00000627068.2:c.507+3C>T	ENSP00000486563.1:n.507+3C>T
NM_014599.5:c.624C>T	NP_055414.2:p.Ala208=
NM_177433.2:c.624C>T	NP_803182.1:p.Ala208=
NM_201222.2:c.624C>T	NP_957516.1:p.Ala208=
NM_177433.3:c.624C>T MANE Select	NP_803182.1:p.Ala208=
NM_014599.6:c.624C>T	NP_055414.2:p.Ala208=
NM_201222.3:c.624C>T	NP_957516.1:p.Ala208=