Canonical Allele Identifier: CA885709574

Gene: MAGI3

Linked Data

• dbSNP Id: rs1419208448
• gnomAD v3: 1-113449259-TCA-T
• gnomAD v4: 1-113449259-TCA-T
• MyVariant Identifiers: chr1:g.113991882_113991883del (hg19) ; chr1:g.113449260_113449261del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113449262_113449263del , CM000663.2:g.113449262_113449263del	GRCh38
NC_000001.10:g.113991884_113991885del , CM000663.1:g.113991884_113991885del	GRCh37
NC_000001.9:g.113793407_113793408del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307546.14:c.316+57913_316+57914del MANE Select	ENSP00000304604.9:n.316+57913_316+57914del
ENST00000307546.13:c.316+57913_316+57914del	ENSP00000304604.9:n.316+57913_316+57914del
ENST00000369611.4:c.316+57913_316+57914del	ENSP00000358624.4:n.316+57913_316+57914del
ENST00000369615.5:c.316+57913_316+57914del	ENSP00000358628.1:n.316+57913_316+57914del
ENST00000369617.8:c.316+57913_316+57914del	ENSP00000358630.4:n.316+57913_316+57914del
ENST00000486456.1:n.219+57913_219+57914del
NM_001142782.1:c.316+57913_316+57914del	NP_001136254.1:n.316+57913_316+57914del
NM_152900.2:c.316+57913_316+57914del	NP_690864.2:n.316+57913_316+57914del
XM_005270737.2:c.316+57913_316+57914del	XP_005270794.1:n.316+57913_316+57914del
XR_946601.1:n.876+57913_876+57914del
XM_005270737.3:c.316+57913_316+57914del	XP_005270794.1:n.316+57913_316+57914del
XM_011541208.2:c.-1941+57913_-1941+57914del	XP_011539510.1:n.-1941+57913_-1941+57914del
XM_017000974.1:c.316+57913_316+57914del	XP_016856463.1:n.316+57913_316+57914del
XR_001737106.1:n.876+57913_876+57914del
XR_946601.2:n.876+57913_876+57914del
NM_001142782.2:c.316+57913_316+57914del MANE Select	NP_001136254.1:n.316+57913_316+57914del
NM_152900.3:c.316+57913_316+57914del	NP_690864.2:n.316+57913_316+57914del