Canonical Allele Identifier: CA1189841714
Gene: MAGI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.113630777_113630809delinsAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGTG , CM000663.2:g.113630777_113630809delinsAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGTG GRCh38
NC_000001.10:g.114173399_114173431delinsAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGTG , CM000663.1:g.114173399_114173431delinsAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGTG GRCh37
NC_000001.9:g.113974922_113974954delinsAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGTG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000307546.14:c.1360+7783_1360+7815delinsAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGTG MANE Select ENSP00000304604.9:n.1360+7783_1360+7815de...
ENST00000307546.13:c.1360+7783_1360+7815delinsAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGTG ENSP00000304604.9:n.1360+7783_1360+7815de...
ENST00000369611.4:c.1360+7783_1360+7815delinsAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGTG ENSP00000358624.4:n.1360+7783_1360+7815de...
ENST00000369615.5:c.1360+7783_1360+7815delinsAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGTG ENSP00000358628.1:n.1360+7783_1360+7815de...
ENST00000369617.8:c.1435+7783_1435+7815delinsAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGTG ENSP00000358630.4:n.1435+7783_1435+7815de...
NM_001142782.1:c.1360+7783_1360+7815delinsAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGTG NP_001136254.1:n.1360+7783_1360+7815delin...
NM_152900.2:c.1360+7783_1360+7815delinsAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGTG NP_690864.2:n.1360+7783_1360+7815delinsAG...
XM_005270737.2:c.1360+7783_1360+7815delinsAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGTG XP_005270794.1:n.1360+7783_1360+7815delin...
XM_011541208.1:c.676+7783_676+7815delinsAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGTG XP_011539510.1:n.676+7783_676+7815delinsA...
XR_946601.1:n.1920+7783_1920+7815delinsAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGTG
XM_005270737.3:c.1360+7783_1360+7815delinsAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGTG XP_005270794.1:n.1360+7783_1360+7815delin...
XM_011541208.2:c.676+7783_676+7815delinsAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGTG XP_011539510.1:n.676+7783_676+7815delinsA...
XM_017000974.1:c.1360+7783_1360+7815delinsAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGTG XP_016856463.1:n.1360+7783_1360+7815delin...
XM_017000975.1:c.187+7783_187+7815delinsAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGTG XP_016856464.1:n.187+7783_187+7815delinsA...
XR_001737106.1:n.1920+7783_1920+7815delinsAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGTG
XR_946601.2:n.1920+7783_1920+7815delinsAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGTG
NM_001142782.2:c.1360+7783_1360+7815delinsAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGTG MANE Select NP_001136254.1:n.1360+7783_1360+7815delin...
NM_152900.3:c.1360+7783_1360+7815delinsAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGTG NP_690864.2:n.1360+7783_1360+7815delinsAG...