Canonical Allele Identifier: CA2603434913
Gene: MAGI3 HGNC NCBI

Linked Data

dbSNP Id: rs2101479979

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.113449113_113449117del , CM000663.2:g.113449113_113449117del GRCh38
NC_000001.10:g.113991735_113991739del , CM000663.1:g.113991735_113991739del GRCh37
NC_000001.9:g.113793258_113793262del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000307546.14:c.316+57764_316+57768del MANE Select ENSP00000304604.9:n.316+57764_316+57768de...
ENST00000307546.13:c.316+57764_316+57768del ENSP00000304604.9:n.316+57764_316+57768de...
ENST00000369611.4:c.316+57764_316+57768del ENSP00000358624.4:n.316+57764_316+57768de...
ENST00000369615.5:c.316+57764_316+57768del ENSP00000358628.1:n.316+57764_316+57768de...
ENST00000369617.8:c.316+57764_316+57768del ENSP00000358630.4:n.316+57764_316+57768de...
ENST00000486456.1:n.219+57764_219+57768del
NM_001142782.1:c.316+57764_316+57768del NP_001136254.1:n.316+57764_316+57768del
NM_152900.2:c.316+57764_316+57768del NP_690864.2:n.316+57764_316+57768del
XM_005270737.2:c.316+57764_316+57768del XP_005270794.1:n.316+57764_316+57768del
XR_946601.1:n.876+57764_876+57768del
XM_005270737.3:c.316+57764_316+57768del XP_005270794.1:n.316+57764_316+57768del
XM_011541208.2:c.-1941+57764_-1941+57768del XP_011539510.1:n.-1941+57764_-1941+57768d...
XM_017000974.1:c.316+57764_316+57768del XP_016856463.1:n.316+57764_316+57768del
XR_001737106.1:n.876+57764_876+57768del
XR_946601.2:n.876+57764_876+57768del
NM_001142782.2:c.316+57764_316+57768del MANE Select NP_001136254.1:n.316+57764_316+57768del
NM_152900.3:c.316+57764_316+57768del NP_690864.2:n.316+57764_316+57768del