Canonical Allele Identifier: CA2430312132
Gene: MAGED2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.54812057T= , CM000685.2:g.54812057T= GRCh38
NC_000023.10:g.54838490T= , CM000685.1:g.54838490T= GRCh37
NC_000023.9:g.54855215T= NCBI36
NG_012844.1:g.9320T=

Transcript Alleles

HGVS Amino-acid change
ENST00000375068.6:c.991-100T= MANE Select ENSP00000364209.1:n.991-100T=
ENST00000218439.8:c.991-100T= ENSP00000218439.4:n.991-100T=
ENST00000347546.8:c.937-100T= ENSP00000336962.4:n.937-100T=
ENST00000375053.6:c.991-100T= ENSP00000364193.2:n.991-100T=
ENST00000375058.5:c.991-100T= ENSP00000364198.1:n.991-100T=
ENST00000375060.5:c.736-100T= ENSP00000364200.1:n.736-100T=
ENST00000375068.5:c.991-100T= ENSP00000364209.1:n.991-100T=
ENST00000396224.1:c.991-100T= ENSP00000379526.1:n.991-100T=
ENST00000487482.5:n.123-100T=
ENST00000627068.2:c.736-100T= ENSP00000486563.1:n.736-100T=
NM_014599.5:c.991-100T= NP_055414.2:n.991-100T=
NM_177433.2:c.991-100T= NP_803182.1:n.991-100T=
NM_201222.2:c.991-100T= NP_957516.1:n.991-100T=
NM_177433.3:c.991-100T= MANE Select NP_803182.1:n.991-100T=
NM_014599.6:c.991-100T= NP_055414.2:n.991-100T=
NM_201222.3:c.991-100T= NP_957516.1:n.991-100T=