Canonical Allele Identifier: CA885709704

Gene: MAGI3

Linked Data

• dbSNP Id: rs71087199
• gnomAD v3: 1-113449360-GGTGTGTGT-G
• gnomAD v4: 1-113449360-GGTGTGTGT-G
• MyVariant Identifiers: chr1:g.113991983_113991990del (hg19) ; chr1:g.113449361_113449368del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113449382_113449389del , CM000663.2:g.113449382_113449389del	GRCh38
NC_000001.10:g.113992004_113992011del , CM000663.1:g.113992004_113992011del	GRCh37
NC_000001.9:g.113793527_113793534del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307546.14:c.316+58033_316+58040del MANE Select	ENSP00000304604.9:n.316+58033_316+58040del
ENST00000307546.13:c.316+58033_316+58040del	ENSP00000304604.9:n.316+58033_316+58040del
ENST00000369611.4:c.316+58033_316+58040del	ENSP00000358624.4:n.316+58033_316+58040del
ENST00000369615.5:c.316+58033_316+58040del	ENSP00000358628.1:n.316+58033_316+58040del
ENST00000369617.8:c.316+58033_316+58040del	ENSP00000358630.4:n.316+58033_316+58040del
ENST00000486456.1:n.219+58033_219+58040del
NM_001142782.1:c.316+58033_316+58040del	NP_001136254.1:n.316+58033_316+58040del
NM_152900.2:c.316+58033_316+58040del	NP_690864.2:n.316+58033_316+58040del
XM_005270737.2:c.316+58033_316+58040del	XP_005270794.1:n.316+58033_316+58040del
XR_946601.1:n.876+58033_876+58040del
XM_005270737.3:c.316+58033_316+58040del	XP_005270794.1:n.316+58033_316+58040del
XM_011541208.2:c.-1941+58033_-1941+58040del	XP_011539510.1:n.-1941+58033_-1941+58040del
XM_017000974.1:c.316+58033_316+58040del	XP_016856463.1:n.316+58033_316+58040del
XR_001737106.1:n.876+58033_876+58040del
XR_946601.2:n.876+58033_876+58040del
NM_001142782.2:c.316+58033_316+58040del MANE Select	NP_001136254.1:n.316+58033_316+58040del
NM_152900.3:c.316+58033_316+58040del	NP_690864.2:n.316+58033_316+58040del