Canonical Allele Identifier: CA1005934164

Gene: MAGI3

Linked Data

• dbSNP Id: rs1654331316
• gnomAD v3: 1-113449108-C-T
• gnomAD v4: 1-113449108-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113449108C>T , CM000663.2:g.113449108C>T	GRCh38
NC_000001.10:g.113991730C>T , CM000663.1:g.113991730C>T	GRCh37
NC_000001.9:g.113793253C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000307546.14:c.316+57759C>T MANE Select	ENSP00000304604.9:n.316+57759C>T
ENST00000307546.13:c.316+57759C>T	ENSP00000304604.9:n.316+57759C>T
ENST00000369611.4:c.316+57759C>T	ENSP00000358624.4:n.316+57759C>T
ENST00000369615.5:c.316+57759C>T	ENSP00000358628.1:n.316+57759C>T
ENST00000369617.8:c.316+57759C>T	ENSP00000358630.4:n.316+57759C>T
ENST00000486456.1:n.219+57759C>T
NM_001142782.1:c.316+57759C>T	NP_001136254.1:n.316+57759C>T
NM_152900.2:c.316+57759C>T	NP_690864.2:n.316+57759C>T
XM_005270737.2:c.316+57759C>T	XP_005270794.1:n.316+57759C>T
XR_946601.1:n.876+57759C>T
XM_005270737.3:c.316+57759C>T	XP_005270794.1:n.316+57759C>T
XM_011541208.2:c.-1941+57759C>T	XP_011539510.1:n.-1941+57759C>T
XM_017000974.1:c.316+57759C>T	XP_016856463.1:n.316+57759C>T
XR_001737106.1:n.876+57759C>T
XR_946601.2:n.876+57759C>T
NM_001142782.2:c.316+57759C>T MANE Select	NP_001136254.1:n.316+57759C>T
NM_152900.3:c.316+57759C>T	NP_690864.2:n.316+57759C>T