Canonical Allele Identifier: CA1189770151
Gene: MAGI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.113449457G= , CM000663.2:g.113449457G= GRCh38
NC_000001.10:g.113992079G= , CM000663.1:g.113992079G= GRCh37
NC_000001.9:g.113793602G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000307546.14:c.316+58108G= MANE Select ENSP00000304604.9:n.316+58108G=
ENST00000307546.13:c.316+58108G= ENSP00000304604.9:n.316+58108G=
ENST00000369611.4:c.316+58108G= ENSP00000358624.4:n.316+58108G=
ENST00000369615.5:c.316+58108G= ENSP00000358628.1:n.316+58108G=
ENST00000369617.8:c.316+58108G= ENSP00000358630.4:n.316+58108G=
ENST00000486456.1:n.219+58108G=
NM_001142782.1:c.316+58108G= NP_001136254.1:n.316+58108G=
NM_152900.2:c.316+58108G= NP_690864.2:n.316+58108G=
XM_005270737.2:c.316+58108G= XP_005270794.1:n.316+58108G=
XR_946601.1:n.876+58108G=
XM_005270737.3:c.316+58108G= XP_005270794.1:n.316+58108G=
XM_011541208.2:c.-1941+58108G= XP_011539510.1:n.-1941+58108G=
XM_017000974.1:c.316+58108G= XP_016856463.1:n.316+58108G=
XR_001737106.1:n.876+58108G=
XR_946601.2:n.876+58108G=
NM_001142782.2:c.316+58108G= MANE Select NP_001136254.1:n.316+58108G=
NM_152900.3:c.316+58108G= NP_690864.2:n.316+58108G=