Canonical Allele Identifier: CA1719128559
Gene: MAGI2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.78041988_78041994delinsAGAGCTG , CM000669.2:g.78041988_78041994delinsAGAGCTG GRCh38
NC_000007.13:g.77671305_77671311delinsAGAGCTG , CM000669.1:g.77671305_77671311delinsAGAGCTG GRCh37
NC_000007.12:g.77509241_77509247delinsAGAGCTG NCBI36
NG_011487.1:g.1416580_1416586delinsCAGCTCT
NG_011487.2:g.1416581_1416587delinsCAGCTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000354212.9:c.3707-22018_3707-22012delinsCAGCTCT MANE Select ENSP00000346151.4:n.3707-22018_3707-22012delinsCAGCTCT
ENST00000635961.1:n.83-6787_83-6781delinsCAGCTCT
ENST00000637441.1:c.3479-22018_3479-22012delinsCAGCTCT ENSP00000489633.1:n.3479-22018_3479-22012delinsCAGCTCT
ENST00000637585.1:c.79-15890_79-15884delinsCAGCTCT ENSP00000490629.1:n.79-15890_79-15884delinsCAGCTCT
ENST00000637976.1:n.28-2363_28-2357delinsCAGCTCT
ENST00000354212.8:c.3707-22018_3707-22012delinsCAGCTCT ENSP00000346151.4:n.3707-22018_3707-22012delinsCAGCTCT
ENST00000419488.5:c.3665-22018_3665-22012delinsCAGCTCT ENSP00000405766.1:n.3665-22018_3665-22012delinsCAGCTCT
ENST00000522391.3:c.3796-22018_3796-22012delinsCAGCTCT ENSP00000428389.1:n.3796-22018_3796-22012delinsCAGCTCT
ENST00000535697.5:c.3251-22018_3251-22012delinsCAGCTCT ENSP00000441603.3:n.3251-22018_3251-22012delinsCAGCTCT
ENST00000626691.2:c.3307-22018_3307-22012delinsCAGCTCT ENSP00000486131.1:n.3307-22018_3307-22012delinsCAGCTCT
ENST00000628980.2:c.3293-22018_3293-22012delinsCAGCTCT ENSP00000487526.1:n.3293-22018_3293-22012delinsCAGCTCT
ENST00000629359.2:c.3265-22018_3265-22012delinsCAGCTCT ENSP00000487448.1:n.3265-22018_3265-22012delinsCAGCTCT
NM_001301128.1:c.3665-22018_3665-22012delinsCAGCTCT NP_001288057.1:n.3665-22018_3665-22012delinsCAGCTCT
NM_012301.3:c.3707-22018_3707-22012delinsCAGCTCT NP_036433.2:n.3707-22018_3707-22012delinsCAGCTCT
XM_011516718.1:c.3796-15890_3796-15884delinsCAGCTCT XP_011515020.1:n.3796-15890_3796-15884delinsCAGCTCT
XM_011516719.1:c.3436-15890_3436-15884delinsCAGCTCT XP_011515021.1:n.3436-15890_3436-15884delinsCAGCTCT
XM_011516720.1:c.3436-15890_3436-15884delinsCAGCTCT XP_011515022.1:n.3436-15890_3436-15884delinsCAGCTCT
XM_011516721.1:c.3265-15890_3265-15884delinsCAGCTCT XP_011515023.1:n.3265-15890_3265-15884delinsCAGCTCT
XM_011516722.1:c.3256-15890_3256-15884delinsCAGCTCT XP_011515024.1:n.3256-15890_3256-15884delinsCAGCTCT
XM_011516723.1:c.3796-22018_3796-22012delinsCAGCTCT XP_011515025.1:n.3796-22018_3796-22012delinsCAGCTCT
XM_011516724.1:c.*50-22018_*50-22012delinsCAGCTCT XP_011515026.1:n.*50-22018_*50-22012delinsCAGCTCT
XM_011516725.1:c.*50-15890_*50-15884delinsCAGCTCT XP_011515027.1:n.*50-15890_*50-15884delinsCAGCTCT
XM_011516726.1:c.2752-15890_2752-15884delinsCAGCTCT XP_011515028.1:n.2752-15890_2752-15884delinsCAGCTCT
XM_011516727.1:c.2752-15890_2752-15884delinsCAGCTCT XP_011515029.1:n.2752-15890_2752-15884delinsCAGCTCT
XM_011516728.1:c.2623-15890_2623-15884delinsCAGCTCT XP_011515030.1:n.2623-15890_2623-15884delinsCAGCTCT
XM_011516729.1:c.2575-15890_2575-15884delinsCAGCTCT XP_011515031.1:n.2575-15890_2575-15884delinsCAGCTCT
XM_011516718.2:c.3796-15890_3796-15884delinsCAGCTCT XP_011515020.1:n.3796-15890_3796-15884delinsCAGCTCT
XM_011516719.3:c.3436-15890_3436-15884delinsCAGCTCT XP_011515021.1:n.3436-15890_3436-15884delinsCAGCTCT
XM_011516720.3:c.3436-15890_3436-15884delinsCAGCTCT XP_011515022.1:n.3436-15890_3436-15884delinsCAGCTCT
XM_011516726.3:c.2752-15890_2752-15884delinsCAGCTCT XP_011515028.1:n.2752-15890_2752-15884delinsCAGCTCT
XM_017012840.2:c.3925-15890_3925-15884delinsCAGCTCT XP_016868329.1:n.3925-15890_3925-15884delinsCAGCTCT
XM_017012841.2:c.3922-15890_3922-15884delinsCAGCTCT XP_016868330.1:n.3922-15890_3922-15884delinsCAGCTCT
XM_017012842.2:c.3919-15890_3919-15884delinsCAGCTCT XP_016868331.1:n.3919-15890_3919-15884delinsCAGCTCT
XM_017012843.2:c.3883-15890_3883-15884delinsCAGCTCT XP_016868332.1:n.3883-15890_3883-15884delinsCAGCTCT
XM_017012844.2:c.3836-22018_3836-22012delinsCAGCTCT XP_016868333.1:n.3836-22018_3836-22012delinsCAGCTCT
XM_017012845.2:c.3790-15890_3790-15884delinsCAGCTCT XP_016868334.1:n.3790-15890_3790-15884delinsCAGCTCT
XM_017012846.2:c.3754-15890_3754-15884delinsCAGCTCT XP_016868335.1:n.3754-15890_3754-15884delinsCAGCTCT
XM_017012847.2:c.3436-15890_3436-15884delinsCAGCTCT XP_016868336.1:n.3436-15890_3436-15884delinsCAGCTCT
XM_017012848.2:c.3307-15890_3307-15884delinsCAGCTCT XP_016868337.1:n.3307-15890_3307-15884delinsCAGCTCT
XM_017012849.2:c.3301-15890_3301-15884delinsCAGCTCT XP_016868338.1:n.3301-15890_3301-15884delinsCAGCTCT
XM_017012850.2:c.3925-22018_3925-22012delinsCAGCTCT XP_016868339.1:n.3925-22018_3925-22012delinsCAGCTCT
XM_017012851.2:c.*50-22018_*50-22012delinsCAGCTCT XP_016868340.1:n.*50-22018_*50-22012delinsCAGCTCT
XM_017012852.2:c.3836-15890_3836-15884delinsCAGCTCT XP_016868341.1:n.3836-15890_3836-15884delinsCAGCTCT
XM_024447009.1:c.3436-15890_3436-15884delinsCAGCTCT XP_024302777.1:n.3436-15890_3436-15884delinsCAGCTCT
NM_012301.4:c.3707-22018_3707-22012delinsCAGCTCT MANE Select NP_036433.2:n.3707-22018_3707-22012delinsCAGCTCT
NM_001301128.2:c.3665-22018_3665-22012delinsCAGCTCT NP_001288057.1:n.3665-22018_3665-22012delinsCAGCTCT