Canonical Allele Identifier: CA1189841718
Gene: MAGI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.113630791G= , CM000663.2:g.113630791G= GRCh38
NC_000001.10:g.114173413G= , CM000663.1:g.114173413G= GRCh37
NC_000001.9:g.113974936G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000307546.14:c.1360+7797G= MANE Select ENSP00000304604.9:n.1360+7797G=
ENST00000307546.13:c.1360+7797G= ENSP00000304604.9:n.1360+7797G=
ENST00000369611.4:c.1360+7797G= ENSP00000358624.4:n.1360+7797G=
ENST00000369615.5:c.1360+7797G= ENSP00000358628.1:n.1360+7797G=
ENST00000369617.8:c.1435+7797G= ENSP00000358630.4:n.1435+7797G=
NM_001142782.1:c.1360+7797G= NP_001136254.1:n.1360+7797G=
NM_152900.2:c.1360+7797G= NP_690864.2:n.1360+7797G=
XM_005270737.2:c.1360+7797G= XP_005270794.1:n.1360+7797G=
XM_011541208.1:c.676+7797G= XP_011539510.1:n.676+7797G=
XR_946601.1:n.1920+7797G=
XM_005270737.3:c.1360+7797G= XP_005270794.1:n.1360+7797G=
XM_011541208.2:c.676+7797G= XP_011539510.1:n.676+7797G=
XM_017000974.1:c.1360+7797G= XP_016856463.1:n.1360+7797G=
XM_017000975.1:c.187+7797G= XP_016856464.1:n.187+7797G=
XR_001737106.1:n.1920+7797G=
XR_946601.2:n.1920+7797G=
NM_001142782.2:c.1360+7797G= MANE Select NP_001136254.1:n.1360+7797G=
NM_152900.3:c.1360+7797G= NP_690864.2:n.1360+7797G=