Canonical Allele Identifier: CA1189819110
Gene: MAGI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.113568414A>T , CM000663.2:g.113568414A>T GRCh38
NC_000001.10:g.114111036A>T , CM000663.1:g.114111036A>T GRCh37
NC_000001.9:g.113912559A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000307546.14:c.434-12128A>T MANE Select ENSP00000304604.9:n.434-12128A>T
ENST00000307546.13:c.434-12128A>T ENSP00000304604.9:n.434-12128A>T
ENST00000369611.4:c.434-12128A>T ENSP00000358624.4:n.434-12128A>T
ENST00000369615.5:c.434-12128A>T ENSP00000358628.1:n.434-12128A>T
ENST00000369617.8:c.434-12128A>T ENSP00000358630.4:n.434-12128A>T
ENST00000486456.1:n.337-12128A>T
NM_001142782.1:c.434-12128A>T NP_001136254.1:n.434-12128A>T
NM_152900.2:c.434-12128A>T NP_690864.2:n.434-12128A>T
XM_005270737.2:c.434-12128A>T XP_005270794.1:n.434-12128A>T
XR_946601.1:n.994-12128A>T
XM_005270737.3:c.434-12128A>T XP_005270794.1:n.434-12128A>T
XM_011541208.2:c.-1823-12128A>T XP_011539510.1:n.-1823-12128A>T
XM_017000974.1:c.434-12128A>T XP_016856463.1:n.434-12128A>T
XR_001737106.1:n.994-12128A>T
XR_946601.2:n.994-12128A>T
NM_001142782.2:c.434-12128A>T MANE Select NP_001136254.1:n.434-12128A>T
NM_152900.3:c.434-12128A>T NP_690864.2:n.434-12128A>T