Canonical Allele Identifier: CA29433985

Gene: MAGI3

Linked Data

• dbSNP Id: rs1025506011
• gnomAD v3: 1-113449438-CAAAT-C
• gnomAD v4: 1-113449438-CAAAT-C
• MyVariant Identifiers: chr1:g.113992061_113992064del (hg19) ; chr1:g.113449439_113449442del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113449439_113449442del , CM000663.2:g.113449439_113449442del	GRCh38
NC_000001.10:g.113992061_113992064del , CM000663.1:g.113992061_113992064del	GRCh37
NC_000001.9:g.113793584_113793587del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307546.14:c.316+58090_316+58093del MANE Select	ENSP00000304604.9:n.316+58090_316+58093del
ENST00000307546.13:c.316+58090_316+58093del	ENSP00000304604.9:n.316+58090_316+58093del
ENST00000369611.4:c.316+58090_316+58093del	ENSP00000358624.4:n.316+58090_316+58093del
ENST00000369615.5:c.316+58090_316+58093del	ENSP00000358628.1:n.316+58090_316+58093del
ENST00000369617.8:c.316+58090_316+58093del	ENSP00000358630.4:n.316+58090_316+58093del
ENST00000486456.1:n.219+58090_219+58093del
NM_001142782.1:c.316+58090_316+58093del	NP_001136254.1:n.316+58090_316+58093del
NM_152900.2:c.316+58090_316+58093del	NP_690864.2:n.316+58090_316+58093del
XM_005270737.2:c.316+58090_316+58093del	XP_005270794.1:n.316+58090_316+58093del
XR_946601.1:n.876+58090_876+58093del
XM_005270737.3:c.316+58090_316+58093del	XP_005270794.1:n.316+58090_316+58093del
XM_011541208.2:c.-1941+58090_-1941+58093del	XP_011539510.1:n.-1941+58090_-1941+58093del
XM_017000974.1:c.316+58090_316+58093del	XP_016856463.1:n.316+58090_316+58093del
XR_001737106.1:n.876+58090_876+58093del
XR_946601.2:n.876+58090_876+58093del
NM_001142782.2:c.316+58090_316+58093del MANE Select	NP_001136254.1:n.316+58090_316+58093del
NM_152900.3:c.316+58090_316+58093del	NP_690864.2:n.316+58090_316+58093del