Canonical Allele Identifier: CA1189770042

Gene: MAGI3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113449362_113449363delinsTG , CM000663.2:g.113449362_113449363delinsTG	GRCh38
NC_000001.10:g.113991984_113991985delinsTG , CM000663.1:g.113991984_113991985delinsTG	GRCh37
NC_000001.9:g.113793507_113793508delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307546.14:c.316+58013_316+58014delinsTG MANE Select	ENSP00000304604.9:n.316+58013_316+58014delinsTG
ENST00000307546.13:c.316+58013_316+58014delinsTG	ENSP00000304604.9:n.316+58013_316+58014delinsTG
ENST00000369611.4:c.316+58013_316+58014delinsTG	ENSP00000358624.4:n.316+58013_316+58014delinsTG
ENST00000369615.5:c.316+58013_316+58014delinsTG	ENSP00000358628.1:n.316+58013_316+58014delinsTG
ENST00000369617.8:c.316+58013_316+58014delinsTG	ENSP00000358630.4:n.316+58013_316+58014delinsTG
ENST00000486456.1:n.219+58013_219+58014delinsTG
NM_001142782.1:c.316+58013_316+58014delinsTG	NP_001136254.1:n.316+58013_316+58014delinsTG
NM_152900.2:c.316+58013_316+58014delinsTG	NP_690864.2:n.316+58013_316+58014delinsTG
XM_005270737.2:c.316+58013_316+58014delinsTG	XP_005270794.1:n.316+58013_316+58014delinsTG
XR_946601.1:n.876+58013_876+58014delinsTG
XM_005270737.3:c.316+58013_316+58014delinsTG	XP_005270794.1:n.316+58013_316+58014delinsTG
XM_011541208.2:c.-1941+58013_-1941+58014delinsTG	XP_011539510.1:n.-1941+58013_-1941+58014delinsTG
XM_017000974.1:c.316+58013_316+58014delinsTG	XP_016856463.1:n.316+58013_316+58014delinsTG
XR_001737106.1:n.876+58013_876+58014delinsTG
XR_946601.2:n.876+58013_876+58014delinsTG
NM_001142782.2:c.316+58013_316+58014delinsTG MANE Select	NP_001136254.1:n.316+58013_316+58014delinsTG
NM_152900.3:c.316+58013_316+58014delinsTG	NP_690864.2:n.316+58013_316+58014delinsTG