Canonical Allele Identifier: CA4313363

Gene: MAGI2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.78019804G>A , CM000669.2:g.78019804G>A	GRCh38
NC_000007.13:g.77649121G>A , CM000669.1:g.77649121G>A	GRCh37
NC_000007.12:g.77487057G>A	NCBI36
NG_011487.1:g.1438770C>T
NG_011487.2:g.1438771C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354212.9:c.3879C>T MANE Select	ENSP00000346151.4:p.Asp1293=
ENST00000637441.1:c.3531+120C>T	ENSP00000489633.1:n.3531+120C>T
ENST00000354212.8:c.3879C>T	ENSP00000346151.4:p.Asp1293=
ENST00000419488.5:c.3837C>T	ENSP00000405766.1:p.Asp1279=
ENST00000522391.3:c.*116C>T	ENSP00000428389.1:n.*116C>T
ENST00000535697.5:c.3423C>T	ENSP00000441603.3:p.Asp1141=
ENST00000626691.2:c.*116C>T	ENSP00000486131.1:n.*116C>T
ENST00000628980.2:c.3465C>T	ENSP00000487526.1:p.Asp1155=
ENST00000629359.2:c.*116C>T	ENSP00000487448.1:n.*116C>T
NM_001301128.1:c.3837C>T	NP_001288057.1:p.Asp1279=
NM_012301.3:c.3879C>T	NP_036433.2:p.Asp1293=
XM_011516718.1:c.4005C>T	XP_011515020.1:p.Asp1335=
XM_011516719.1:c.3645C>T	XP_011515021.1:p.Asp1215=
XM_011516720.1:c.3645C>T	XP_011515022.1:p.Asp1215=
XM_011516721.1:c.3474C>T	XP_011515023.1:p.Asp1158=
XM_011516722.1:c.3465C>T	XP_011515024.1:p.Asp1155=
XM_011516723.1:c.*116C>T	XP_011515025.1:n.*116C>T
XM_011516726.1:c.2961C>T	XP_011515028.1:p.Asp987=
XM_011516727.1:c.2961C>T	XP_011515029.1:p.Asp987=
XM_011516728.1:c.2832C>T	XP_011515030.1:p.Asp944=
XM_011516729.1:c.2784C>T	XP_011515031.1:p.Asp928=
XM_011516718.2:c.4005C>T	XP_011515020.1:p.Asp1335=
XM_011516719.3:c.3645C>T	XP_011515021.1:p.Asp1215=
XM_011516720.3:c.3645C>T	XP_011515022.1:p.Asp1215=
XM_011516726.3:c.2961C>T	XP_011515028.1:p.Asp987=
XM_017012840.2:c.4134C>T	XP_016868329.1:p.Asp1378=
XM_017012841.2:c.4131C>T	XP_016868330.1:p.Asp1377=
XM_017012842.2:c.4128C>T	XP_016868331.1:p.Asp1376=
XM_017012843.2:c.4092C>T	XP_016868332.1:p.Asp1364=
XM_017012844.2:c.4008C>T	XP_016868333.1:p.Asp1336=
XM_017012845.2:c.3999C>T	XP_016868334.1:p.Asp1333=
XM_017012846.2:c.3963C>T	XP_016868335.1:p.Asp1321=
XM_017012847.2:c.3645C>T	XP_016868336.1:p.Asp1215=
XM_017012848.2:c.3516C>T	XP_016868337.1:p.Asp1172=
XM_017012849.2:c.3510C>T	XP_016868338.1:p.Asp1170=
XM_017012850.2:c.*116C>T	XP_016868339.1:n.*116C>T
XM_024447009.1:c.3645C>T	XP_024302777.1:p.Asp1215=
NM_012301.4:c.3879C>T MANE Select	NP_036433.2:p.Asp1293=
NM_001301128.2:c.3837C>T	NP_001288057.1:p.Asp1279=