Canonical Allele Identifier: CA2430312143
Gene: MAGED2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.54812078_54812079delinsCT , CM000685.2:g.54812078_54812079delinsCT GRCh38
NC_000023.10:g.54838511_54838512delinsCT , CM000685.1:g.54838511_54838512delinsCT GRCh37
NC_000023.9:g.54855236_54855237delinsCT NCBI36
NG_012844.1:g.9341_9342delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000375068.6:c.991-79_991-78delinsCT MANE Select ENSP00000364209.1:n.991-79_991-78delinsCT
ENST00000218439.8:c.991-79_991-78delinsCT ENSP00000218439.4:n.991-79_991-78delinsCT
ENST00000347546.8:c.937-79_937-78delinsCT ENSP00000336962.4:n.937-79_937-78delinsCT
ENST00000375053.6:c.991-79_991-78delinsCT ENSP00000364193.2:n.991-79_991-78delinsCT
ENST00000375058.5:c.991-79_991-78delinsCT ENSP00000364198.1:n.991-79_991-78delinsCT
ENST00000375060.5:c.736-79_736-78delinsCT ENSP00000364200.1:n.736-79_736-78delinsCT
ENST00000375068.5:c.991-79_991-78delinsCT ENSP00000364209.1:n.991-79_991-78delinsCT
ENST00000396224.1:c.991-79_991-78delinsCT ENSP00000379526.1:n.991-79_991-78delinsCT
ENST00000487482.5:n.123-79_123-78delinsCT
ENST00000627068.2:c.736-79_736-78delinsCT ENSP00000486563.1:n.736-79_736-78delinsCT
NM_014599.5:c.991-79_991-78delinsCT NP_055414.2:n.991-79_991-78delinsCT
NM_177433.2:c.991-79_991-78delinsCT NP_803182.1:n.991-79_991-78delinsCT
NM_201222.2:c.991-79_991-78delinsCT NP_957516.1:n.991-79_991-78delinsCT
NM_177433.3:c.991-79_991-78delinsCT MANE Select NP_803182.1:n.991-79_991-78delinsCT
NM_014599.6:c.991-79_991-78delinsCT NP_055414.2:n.991-79_991-78delinsCT
NM_201222.3:c.991-79_991-78delinsCT NP_957516.1:n.991-79_991-78delinsCT