Canonical Allele Identifier: CA2563825587

Gene: MAGI3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113449367_113449368insGGTGTG , CM000663.2:g.113449367_113449368insGGTGTG	GRCh38
NC_000001.10:g.113991989_113991990insGGTGTG , CM000663.1:g.113991989_113991990insGGTGTG	GRCh37
NC_000001.9:g.113793512_113793513insGGTGTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307546.14:c.316+58018_316+58019insGGTGTG MANE Select	ENSP00000304604.9:n.316+58018_316+58019insGGTGTG
ENST00000307546.13:c.316+58018_316+58019insGGTGTG	ENSP00000304604.9:n.316+58018_316+58019insGGTGTG
ENST00000369611.4:c.316+58018_316+58019insGGTGTG	ENSP00000358624.4:n.316+58018_316+58019insGGTGTG
ENST00000369615.5:c.316+58018_316+58019insGGTGTG	ENSP00000358628.1:n.316+58018_316+58019insGGTGTG
ENST00000369617.8:c.316+58018_316+58019insGGTGTG	ENSP00000358630.4:n.316+58018_316+58019insGGTGTG
ENST00000486456.1:n.219+58018_219+58019insGGTGTG
NM_001142782.1:c.316+58018_316+58019insGGTGTG	NP_001136254.1:n.316+58018_316+58019insGGTGTG
NM_152900.2:c.316+58018_316+58019insGGTGTG	NP_690864.2:n.316+58018_316+58019insGGTGTG
XM_005270737.2:c.316+58018_316+58019insGGTGTG	XP_005270794.1:n.316+58018_316+58019insGGTGTG
XR_946601.1:n.876+58018_876+58019insGGTGTG
XM_005270737.3:c.316+58018_316+58019insGGTGTG	XP_005270794.1:n.316+58018_316+58019insGGTGTG
XM_011541208.2:c.-1941+58018_-1941+58019insGGTGTG	XP_011539510.1:n.-1941+58018_-1941+58019insGGTGTG
XM_017000974.1:c.316+58018_316+58019insGGTGTG	XP_016856463.1:n.316+58018_316+58019insGGTGTG
XR_001737106.1:n.876+58018_876+58019insGGTGTG
XR_946601.2:n.876+58018_876+58019insGGTGTG
NM_001142782.2:c.316+58018_316+58019insGGTGTG MANE Select	NP_001136254.1:n.316+58018_316+58019insGGTGTG
NM_152900.3:c.316+58018_316+58019insGGTGTG	NP_690864.2:n.316+58018_316+58019insGGTGTG