Canonical Allele Identifier: CA1719200821
Gene: MAGI2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.78209192_78209193delinsAC , CM000669.2:g.78209192_78209193delinsAC GRCh38
NC_000007.13:g.77838509_77838510delinsAC , CM000669.1:g.77838509_77838510delinsAC GRCh37
NC_000007.12:g.77676445_77676446delinsAC NCBI36
NG_011487.1:g.1249381_1249382delinsGT
NG_011487.2:g.1249382_1249383delinsGT

Transcript Alleles

HGVS Amino-acid change
ENST00000354212.9:c.2048-8000_2048-7999delinsGT MANE Select ENSP00000346151.4:n.2048-8000_2048-7999delinsGT
ENST00000636178.1:c.1118-8000_1118-7999delinsGT ENSP00000489709.1:n.1118-8000_1118-7999delinsGT
ENST00000637282.1:c.875-8000_875-7999delinsGT ENSP00000490637.1:n.875-8000_875-7999delinsGT
ENST00000637441.1:c.2048-8000_2048-7999delinsGT ENSP00000489633.1:n.2048-8000_2048-7999delinsGT
ENST00000637486.1:c.*150-8000_*150-7999delinsGT ENSP00000490080.1:n.*150-8000_*150-7999delinsGT
ENST00000354212.8:c.2048-8000_2048-7999delinsGT ENSP00000346151.4:n.2048-8000_2048-7999delinsGT
ENST00000419488.5:c.2048-8000_2048-7999delinsGT ENSP00000405766.1:n.2048-8000_2048-7999delinsGT
ENST00000519748.5:c.875-8000_875-7999delinsGT ENSP00000486774.1:n.875-8000_875-7999delinsGT
ENST00000520379.2:n.1123-8000_1123-7999delinsGT
ENST00000522391.3:c.2048-8000_2048-7999delinsGT ENSP00000428389.1:n.2048-8000_2048-7999delinsGT
ENST00000535697.5:c.1634-8000_1634-7999delinsGT ENSP00000441603.3:n.1634-8000_1634-7999delinsGT
ENST00000626691.2:c.1559-8000_1559-7999delinsGT ENSP00000486131.1:n.1559-8000_1559-7999delinsGT
ENST00000628980.2:c.1634-8000_1634-7999delinsGT ENSP00000487526.1:n.1634-8000_1634-7999delinsGT
ENST00000629359.2:c.1559-8000_1559-7999delinsGT ENSP00000487448.1:n.1559-8000_1559-7999delinsGT
NM_001301128.1:c.2048-8000_2048-7999delinsGT NP_001288057.1:n.2048-8000_2048-7999delinsGT
NM_012301.3:c.2048-8000_2048-7999delinsGT NP_036433.2:n.2048-8000_2048-7999delinsGT
XM_011516718.1:c.2048-8000_2048-7999delinsGT XP_011515020.1:n.2048-8000_2048-7999delinsGT
XM_011516719.1:c.1688-8000_1688-7999delinsGT XP_011515021.1:n.1688-8000_1688-7999delinsGT
XM_011516720.1:c.1688-8000_1688-7999delinsGT XP_011515022.1:n.1688-8000_1688-7999delinsGT
XM_011516721.1:c.1559-8000_1559-7999delinsGT XP_011515023.1:n.1559-8000_1559-7999delinsGT
XM_011516722.1:c.1508-8000_1508-7999delinsGT XP_011515024.1:n.1508-8000_1508-7999delinsGT
XM_011516723.1:c.2048-8000_2048-7999delinsGT XP_011515025.1:n.2048-8000_2048-7999delinsGT
XM_011516724.1:c.2048-8000_2048-7999delinsGT XP_011515026.1:n.2048-8000_2048-7999delinsGT
XM_011516725.1:c.2048-8000_2048-7999delinsGT XP_011515027.1:n.2048-8000_2048-7999delinsGT
XM_011516726.1:c.1004-8000_1004-7999delinsGT XP_011515028.1:n.1004-8000_1004-7999delinsGT
XM_011516727.1:c.1004-8000_1004-7999delinsGT XP_011515029.1:n.1004-8000_1004-7999delinsGT
XM_011516728.1:c.875-8000_875-7999delinsGT XP_011515030.1:n.875-8000_875-7999delinsGT
XM_011516729.1:c.875-8000_875-7999delinsGT XP_011515031.1:n.875-8000_875-7999delinsGT
XR_927699.1:n.149-3161_149-3160delinsAC
XM_011516718.2:c.2048-8000_2048-7999delinsGT XP_011515020.1:n.2048-8000_2048-7999delinsGT
XM_011516719.3:c.1688-8000_1688-7999delinsGT XP_011515021.1:n.1688-8000_1688-7999delinsGT
XM_011516720.3:c.1688-8000_1688-7999delinsGT XP_011515022.1:n.1688-8000_1688-7999delinsGT
XM_011516726.3:c.1004-8000_1004-7999delinsGT XP_011515028.1:n.1004-8000_1004-7999delinsGT
XM_017012840.2:c.2177-8000_2177-7999delinsGT XP_016868329.1:n.2177-8000_2177-7999delinsGT
XM_017012841.2:c.2174-8000_2174-7999delinsGT XP_016868330.1:n.2174-8000_2174-7999delinsGT
XM_017012842.2:c.2177-8000_2177-7999delinsGT XP_016868331.1:n.2177-8000_2177-7999delinsGT
XM_017012843.2:c.2177-8000_2177-7999delinsGT XP_016868332.1:n.2177-8000_2177-7999delinsGT
XM_017012844.2:c.2177-8000_2177-7999delinsGT XP_016868333.1:n.2177-8000_2177-7999delinsGT
XM_017012845.2:c.2048-8000_2048-7999delinsGT XP_016868334.1:n.2048-8000_2048-7999delinsGT
XM_017012846.2:c.2048-8000_2048-7999delinsGT XP_016868335.1:n.2048-8000_2048-7999delinsGT
XM_017012847.2:c.1688-8000_1688-7999delinsGT XP_016868336.1:n.1688-8000_1688-7999delinsGT
XM_017012848.2:c.1559-8000_1559-7999delinsGT XP_016868337.1:n.1559-8000_1559-7999delinsGT
XM_017012849.2:c.1559-8000_1559-7999delinsGT XP_016868338.1:n.1559-8000_1559-7999delinsGT
XM_017012850.2:c.2177-8000_2177-7999delinsGT XP_016868339.1:n.2177-8000_2177-7999delinsGT
XM_017012851.2:c.2177-8000_2177-7999delinsGT XP_016868340.1:n.2177-8000_2177-7999delinsGT
XM_017012852.2:c.2177-8000_2177-7999delinsGT XP_016868341.1:n.2177-8000_2177-7999delinsGT
XM_024447009.1:c.1688-8000_1688-7999delinsGT XP_024302777.1:n.1688-8000_1688-7999delinsGT
NM_012301.4:c.2048-8000_2048-7999delinsGT MANE Select NP_036433.2:n.2048-8000_2048-7999delinsGT
NM_001301128.2:c.2048-8000_2048-7999delinsGT NP_001288057.1:n.2048-8000_2048-7999delinsGT