Canonical Allele Identifier: CA1189841707

Gene: MAGI3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113630774_113630776delinsACC , CM000663.2:g.113630774_113630776delinsACC	GRCh38
NC_000001.10:g.114173396_114173398delinsACC , CM000663.1:g.114173396_114173398delinsACC	GRCh37
NC_000001.9:g.113974919_113974921delinsACC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307546.14:c.1360+7780_1360+7782delinsACC MANE Select	ENSP00000304604.9:n.1360+7780_1360+7782delinsACC
ENST00000307546.13:c.1360+7780_1360+7782delinsACC	ENSP00000304604.9:n.1360+7780_1360+7782delinsACC
ENST00000369611.4:c.1360+7780_1360+7782delinsACC	ENSP00000358624.4:n.1360+7780_1360+7782delinsACC
ENST00000369615.5:c.1360+7780_1360+7782delinsACC	ENSP00000358628.1:n.1360+7780_1360+7782delinsACC
ENST00000369617.8:c.1435+7780_1435+7782delinsACC	ENSP00000358630.4:n.1435+7780_1435+7782delinsACC
NM_001142782.1:c.1360+7780_1360+7782delinsACC	NP_001136254.1:n.1360+7780_1360+7782delinsACC
NM_152900.2:c.1360+7780_1360+7782delinsACC	NP_690864.2:n.1360+7780_1360+7782delinsACC
XM_005270737.2:c.1360+7780_1360+7782delinsACC	XP_005270794.1:n.1360+7780_1360+7782delinsACC
XM_011541208.1:c.676+7780_676+7782delinsACC	XP_011539510.1:n.676+7780_676+7782delinsACC
XR_946601.1:n.1920+7780_1920+7782delinsACC
XM_005270737.3:c.1360+7780_1360+7782delinsACC	XP_005270794.1:n.1360+7780_1360+7782delinsACC
XM_011541208.2:c.676+7780_676+7782delinsACC	XP_011539510.1:n.676+7780_676+7782delinsACC
XM_017000974.1:c.1360+7780_1360+7782delinsACC	XP_016856463.1:n.1360+7780_1360+7782delinsACC
XM_017000975.1:c.187+7780_187+7782delinsACC	XP_016856464.1:n.187+7780_187+7782delinsACC
XR_001737106.1:n.1920+7780_1920+7782delinsACC
XR_946601.2:n.1920+7780_1920+7782delinsACC
NM_001142782.2:c.1360+7780_1360+7782delinsACC MANE Select	NP_001136254.1:n.1360+7780_1360+7782delinsACC
NM_152900.3:c.1360+7780_1360+7782delinsACC	NP_690864.2:n.1360+7780_1360+7782delinsACC