Canonical Allele Identifier: CA1005934476
Gene: MAGI3 HGNC NCBI

Linked Data

dbSNP Id: rs1654368132

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.113449468_113449471del , CM000663.2:g.113449468_113449471del GRCh38
NC_000001.10:g.113992090_113992093del , CM000663.1:g.113992090_113992093del GRCh37
NC_000001.9:g.113793613_113793616del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000307546.14:c.316+58119_316+58122del MANE Select ENSP00000304604.9:n.316+58119_316+58122del
ENST00000307546.13:c.316+58119_316+58122del ENSP00000304604.9:n.316+58119_316+58122del
ENST00000369611.4:c.316+58119_316+58122del ENSP00000358624.4:n.316+58119_316+58122del
ENST00000369615.5:c.316+58119_316+58122del ENSP00000358628.1:n.316+58119_316+58122del
ENST00000369617.8:c.316+58119_316+58122del ENSP00000358630.4:n.316+58119_316+58122del
ENST00000486456.1:n.219+58119_219+58122del
NM_001142782.1:c.316+58119_316+58122del NP_001136254.1:n.316+58119_316+58122del
NM_152900.2:c.316+58119_316+58122del NP_690864.2:n.316+58119_316+58122del
XM_005270737.2:c.316+58119_316+58122del XP_005270794.1:n.316+58119_316+58122del
XR_946601.1:n.876+58119_876+58122del
XM_005270737.3:c.316+58119_316+58122del XP_005270794.1:n.316+58119_316+58122del
XM_011541208.2:c.-1941+58119_-1941+58122del XP_011539510.1:n.-1941+58119_-1941+58122del
XM_017000974.1:c.316+58119_316+58122del XP_016856463.1:n.316+58119_316+58122del
XR_001737106.1:n.876+58119_876+58122del
XR_946601.2:n.876+58119_876+58122del
NM_001142782.2:c.316+58119_316+58122del MANE Select NP_001136254.1:n.316+58119_316+58122del
NM_152900.3:c.316+58119_316+58122del NP_690864.2:n.316+58119_316+58122del