Canonical Allele Identifier: CA885709741
Gene: MAGI3 HGNC NCBI

Linked Data

dbSNP Id: rs1193089061

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.113449368_113449369insTTGTGT , CM000663.2:g.113449368_113449369insTTGTGT GRCh38
NC_000001.10:g.113991990_113991991insTTGTGT , CM000663.1:g.113991990_113991991insTTGTGT GRCh37
NC_000001.9:g.113793513_113793514insTTGTGT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000307546.14:c.316+58019_316+58020insTTGTGT MANE Select ENSP00000304604.9:n.316+58019_316+58020insTTGTGT
ENST00000307546.13:c.316+58019_316+58020insTTGTGT ENSP00000304604.9:n.316+58019_316+58020insTTGTGT
ENST00000369611.4:c.316+58019_316+58020insTTGTGT ENSP00000358624.4:n.316+58019_316+58020insTTGTGT
ENST00000369615.5:c.316+58019_316+58020insTTGTGT ENSP00000358628.1:n.316+58019_316+58020insTTGTGT
ENST00000369617.8:c.316+58019_316+58020insTTGTGT ENSP00000358630.4:n.316+58019_316+58020insTTGTGT
ENST00000486456.1:n.219+58019_219+58020insTTGTGT
NM_001142782.1:c.316+58019_316+58020insTTGTGT NP_001136254.1:n.316+58019_316+58020insTTGTGT
NM_152900.2:c.316+58019_316+58020insTTGTGT NP_690864.2:n.316+58019_316+58020insTTGTGT
XM_005270737.2:c.316+58019_316+58020insTTGTGT XP_005270794.1:n.316+58019_316+58020insTTGTGT
XR_946601.1:n.876+58019_876+58020insTTGTGT
XM_005270737.3:c.316+58019_316+58020insTTGTGT XP_005270794.1:n.316+58019_316+58020insTTGTGT
XM_011541208.2:c.-1941+58019_-1941+58020insTTGTGT XP_011539510.1:n.-1941+58019_-1941+58020insTTGTGT
XM_017000974.1:c.316+58019_316+58020insTTGTGT XP_016856463.1:n.316+58019_316+58020insTTGTGT
XR_001737106.1:n.876+58019_876+58020insTTGTGT
XR_946601.2:n.876+58019_876+58020insTTGTGT
NM_001142782.2:c.316+58019_316+58020insTTGTGT MANE Select NP_001136254.1:n.316+58019_316+58020insTTGTGT
NM_152900.3:c.316+58019_316+58020insTTGTGT NP_690864.2:n.316+58019_316+58020insTTGTGT