Canonical Allele Identifier: CA2430312177
Gene: MAGED2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.54812163G= , CM000685.2:g.54812163G= GRCh38
NC_000023.10:g.54838596G= , CM000685.1:g.54838596G= GRCh37
NC_000023.9:g.54855321G= NCBI36
NG_012844.1:g.9426G=

Transcript Alleles

HGVS Amino-acid change
ENST00000375068.6:c.997G= MANE Select ENSP00000364209.1:p.Gly333=
ENST00000218439.8:c.997G= ENSP00000218439.4:p.Gly333=
ENST00000347546.8:c.943G= ENSP00000336962.4:p.Gly315=
ENST00000375053.6:c.997G= ENSP00000364193.2:p.Gly333=
ENST00000375058.5:c.997G= ENSP00000364198.1:p.Gly333=
ENST00000375060.5:c.742G= ENSP00000364200.1:p.Gly248=
ENST00000375068.5:c.997G= ENSP00000364209.1:p.Gly333=
ENST00000396224.1:c.997G= ENSP00000379526.1:p.Gly333=
ENST00000487482.5:n.129G=
ENST00000627068.2:c.742G= ENSP00000486563.1:p.Gly248=
NM_014599.5:c.997G= NP_055414.2:p.Gly333=
NM_177433.2:c.997G= NP_803182.1:p.Gly333=
NM_201222.2:c.997G= NP_957516.1:p.Gly333=
NM_177433.3:c.997G= MANE Select NP_803182.1:p.Gly333=
NM_014599.6:c.997G= NP_055414.2:p.Gly333=
NM_201222.3:c.997G= NP_957516.1:p.Gly333=