Canonical Allele Identifier: CA1189841706

Gene: MAGI3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113630774_113630808delinsACCAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGT , CM000663.2:g.113630774_113630808delinsACCAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGT	GRCh38
NC_000001.10:g.114173396_114173430delinsACCAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGT , CM000663.1:g.114173396_114173430delinsACCAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGT	GRCh37
NC_000001.9:g.113974919_113974953delinsACCAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000307546.14:c.1360+7780_1360+7814delinsACCAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGT MANE Select	ENSP00000304604.9:n.1360+7780_1360+7814de...
ENST00000307546.13:c.1360+7780_1360+7814delinsACCAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGT	ENSP00000304604.9:n.1360+7780_1360+7814de...
ENST00000369611.4:c.1360+7780_1360+7814delinsACCAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGT	ENSP00000358624.4:n.1360+7780_1360+7814de...
ENST00000369615.5:c.1360+7780_1360+7814delinsACCAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGT	ENSP00000358628.1:n.1360+7780_1360+7814de...
ENST00000369617.8:c.1435+7780_1435+7814delinsACCAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGT	ENSP00000358630.4:n.1435+7780_1435+7814de...
NM_001142782.1:c.1360+7780_1360+7814delinsACCAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGT	NP_001136254.1:n.1360+7780_1360+7814delin...
NM_152900.2:c.1360+7780_1360+7814delinsACCAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGT	NP_690864.2:n.1360+7780_1360+7814delinsAC...
XM_005270737.2:c.1360+7780_1360+7814delinsACCAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGT	XP_005270794.1:n.1360+7780_1360+7814delin...
XM_011541208.1:c.676+7780_676+7814delinsACCAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGT	XP_011539510.1:n.676+7780_676+7814delinsA...
XR_946601.1:n.1920+7780_1920+7814delinsACCAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGT
XM_005270737.3:c.1360+7780_1360+7814delinsACCAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGT	XP_005270794.1:n.1360+7780_1360+7814delin...
XM_011541208.2:c.676+7780_676+7814delinsACCAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGT	XP_011539510.1:n.676+7780_676+7814delinsA...
XM_017000974.1:c.1360+7780_1360+7814delinsACCAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGT	XP_016856463.1:n.1360+7780_1360+7814delin...
XM_017000975.1:c.187+7780_187+7814delinsACCAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGT	XP_016856464.1:n.187+7780_187+7814delinsA...
XR_001737106.1:n.1920+7780_1920+7814delinsACCAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGT
XR_946601.2:n.1920+7780_1920+7814delinsACCAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGT
NM_001142782.2:c.1360+7780_1360+7814delinsACCAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGT MANE Select	NP_001136254.1:n.1360+7780_1360+7814delin...
NM_152900.3:c.1360+7780_1360+7814delinsACCAGGTGGCTGCTACCGGGAGCTAAGGGAGAGGT	NP_690864.2:n.1360+7780_1360+7814delinsAC...