Canonical Allele Identifier: CA1189769922

Gene: MAGI3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113449272_113449273delinsGC , CM000663.2:g.113449272_113449273delinsGC	GRCh38
NC_000001.10:g.113991894_113991895delinsGC , CM000663.1:g.113991894_113991895delinsGC	GRCh37
NC_000001.9:g.113793417_113793418delinsGC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307546.14:c.316+57923_316+57924delinsGC MANE Select	ENSP00000304604.9:n.316+57923_316+57924delinsGC
ENST00000307546.13:c.316+57923_316+57924delinsGC	ENSP00000304604.9:n.316+57923_316+57924delinsGC
ENST00000369611.4:c.316+57923_316+57924delinsGC	ENSP00000358624.4:n.316+57923_316+57924delinsGC
ENST00000369615.5:c.316+57923_316+57924delinsGC	ENSP00000358628.1:n.316+57923_316+57924delinsGC
ENST00000369617.8:c.316+57923_316+57924delinsGC	ENSP00000358630.4:n.316+57923_316+57924delinsGC
ENST00000486456.1:n.219+57923_219+57924delinsGC
NM_001142782.1:c.316+57923_316+57924delinsGC	NP_001136254.1:n.316+57923_316+57924delinsGC
NM_152900.2:c.316+57923_316+57924delinsGC	NP_690864.2:n.316+57923_316+57924delinsGC
XM_005270737.2:c.316+57923_316+57924delinsGC	XP_005270794.1:n.316+57923_316+57924delinsGC
XR_946601.1:n.876+57923_876+57924delinsGC
XM_005270737.3:c.316+57923_316+57924delinsGC	XP_005270794.1:n.316+57923_316+57924delinsGC
XM_011541208.2:c.-1941+57923_-1941+57924delinsGC	XP_011539510.1:n.-1941+57923_-1941+57924delinsGC
XM_017000974.1:c.316+57923_316+57924delinsGC	XP_016856463.1:n.316+57923_316+57924delinsGC
XR_001737106.1:n.876+57923_876+57924delinsGC
XR_946601.2:n.876+57923_876+57924delinsGC
NM_001142782.2:c.316+57923_316+57924delinsGC MANE Select	NP_001136254.1:n.316+57923_316+57924delinsGC
NM_152900.3:c.316+57923_316+57924delinsGC	NP_690864.2:n.316+57923_316+57924delinsGC