Canonical Allele Identifier: CA885709857

Gene: MAGI3

Linked Data

• dbSNP Id: rs1257220627
• gnomAD v3: 1-113449431-G-GA
• gnomAD v4: 1-113449431-G-GA
• MyVariant Identifiers: chr1:g.113992053_113992054insA (hg19) ; chr1:g.113449431_113449432insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113449437dup , CM000663.2:g.113449437dup	GRCh38
NC_000001.10:g.113992059dup , CM000663.1:g.113992059dup	GRCh37
NC_000001.9:g.113793582dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307546.14:c.316+58088dup MANE Select	ENSP00000304604.9:n.316+58088dup
ENST00000307546.13:c.316+58088dup	ENSP00000304604.9:n.316+58088dup
ENST00000369611.4:c.316+58088dup	ENSP00000358624.4:n.316+58088dup
ENST00000369615.5:c.316+58088dup	ENSP00000358628.1:n.316+58088dup
ENST00000369617.8:c.316+58088dup	ENSP00000358630.4:n.316+58088dup
ENST00000486456.1:n.219+58088dup
NM_001142782.1:c.316+58088dup	NP_001136254.1:n.316+58088dup
NM_152900.2:c.316+58088dup	NP_690864.2:n.316+58088dup
XM_005270737.2:c.316+58088dup	XP_005270794.1:n.316+58088dup
XR_946601.1:n.876+58088dup
XM_005270737.3:c.316+58088dup	XP_005270794.1:n.316+58088dup
XM_011541208.2:c.-1941+58088dup	XP_011539510.1:n.-1941+58088dup
XM_017000974.1:c.316+58088dup	XP_016856463.1:n.316+58088dup
XR_001737106.1:n.876+58088dup
XR_946601.2:n.876+58088dup
NM_001142782.2:c.316+58088dup MANE Select	NP_001136254.1:n.316+58088dup
NM_152900.3:c.316+58088dup	NP_690864.2:n.316+58088dup