Canonical Allele Identifier: CA29433974

Gene: MAGI3

Linked Data

• dbSNP Id: rs1019483983
• gnomAD v2: 1-113992000-T-TGC
• gnomAD v3: 1-113449378-T-TGC
• gnomAD v4: 1-113449378-T-TGC
• MyVariant Identifiers: chr1:g.113992000_113992001insGC (hg19) ; chr1:g.113449378_113449379insGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113449379_113449380insCG , CM000663.2:g.113449379_113449380insCG	GRCh38
NC_000001.10:g.113992001_113992002insCG , CM000663.1:g.113992001_113992002insCG	GRCh37
NC_000001.9:g.113793524_113793525insCG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307546.14:c.316+58030_316+58031insCG MANE Select	ENSP00000304604.9:n.316+58030_316+58031insCG
ENST00000307546.13:c.316+58030_316+58031insCG	ENSP00000304604.9:n.316+58030_316+58031insCG
ENST00000369611.4:c.316+58030_316+58031insCG	ENSP00000358624.4:n.316+58030_316+58031insCG
ENST00000369615.5:c.316+58030_316+58031insCG	ENSP00000358628.1:n.316+58030_316+58031insCG
ENST00000369617.8:c.316+58030_316+58031insCG	ENSP00000358630.4:n.316+58030_316+58031insCG
ENST00000486456.1:n.219+58030_219+58031insCG
NM_001142782.1:c.316+58030_316+58031insCG	NP_001136254.1:n.316+58030_316+58031insCG
NM_152900.2:c.316+58030_316+58031insCG	NP_690864.2:n.316+58030_316+58031insCG
XM_005270737.2:c.316+58030_316+58031insCG	XP_005270794.1:n.316+58030_316+58031insCG
XR_946601.1:n.876+58030_876+58031insCG
XM_005270737.3:c.316+58030_316+58031insCG	XP_005270794.1:n.316+58030_316+58031insCG
XM_011541208.2:c.-1941+58030_-1941+58031insCG	XP_011539510.1:n.-1941+58030_-1941+58031insCG
XM_017000974.1:c.316+58030_316+58031insCG	XP_016856463.1:n.316+58030_316+58031insCG
XR_001737106.1:n.876+58030_876+58031insCG
XR_946601.2:n.876+58030_876+58031insCG
NM_001142782.2:c.316+58030_316+58031insCG MANE Select	NP_001136254.1:n.316+58030_316+58031insCG
NM_152900.3:c.316+58030_316+58031insCG	NP_690864.2:n.316+58030_316+58031insCG