Canonical Allele Identifier: CA4313460

Gene: MAGI2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.78078966C>T , CM000669.2:g.78078966C>T	GRCh38
NC_000007.13:g.77708283C>T , CM000669.1:g.77708283C>T	GRCh37
NC_000007.12:g.77546219C>T	NCBI36
NG_011487.1:g.1379608G>A
NG_011487.2:g.1379609G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354212.9:c.3687G>A MANE Select	ENSP00000346151.4:p.Thr1229=
ENST00000637282.1:c.2466G>A	ENSP00000490637.1:p.Thr822=
ENST00000637441.1:c.3459G>A	ENSP00000489633.1:p.Thr1153=
ENST00000637486.1:c.*1789G>A	ENSP00000490080.1:n.*1789G>A
ENST00000637976.1:n.8G>A
ENST00000354212.8:c.3687G>A	ENSP00000346151.4:p.Thr1229=
ENST00000419488.5:c.3645G>A	ENSP00000405766.1:p.Thr1215=
ENST00000519748.5:c.2466G>A	ENSP00000486774.1:p.Thr822=
ENST00000522391.3:c.3687G>A	ENSP00000428389.1:p.Thr1229=
ENST00000535697.5:c.3231G>A	ENSP00000441603.3:p.Thr1077=
ENST00000626691.2:c.3198G>A	ENSP00000486131.1:p.Thr1066=
ENST00000628980.2:c.3273G>A	ENSP00000487526.1:p.Thr1091=
ENST00000629359.2:c.3156G>A	ENSP00000487448.1:p.Thr1052=
NM_001301128.1:c.3645G>A	NP_001288057.1:p.Thr1215=
NM_012301.3:c.3687G>A	NP_036433.2:p.Thr1229=
XM_011516718.1:c.3687G>A	XP_011515020.1:p.Thr1229=
XM_011516719.1:c.3327G>A	XP_011515021.1:p.Thr1109=
XM_011516720.1:c.3327G>A	XP_011515022.1:p.Thr1109=
XM_011516721.1:c.3156G>A	XP_011515023.1:p.Thr1052=
XM_011516722.1:c.3147G>A	XP_011515024.1:p.Thr1049=
XM_011516723.1:c.3687G>A	XP_011515025.1:p.Thr1229=
XM_011516724.1:c.3687G>A	XP_011515026.1:p.Thr1229=
XM_011516725.1:c.3687G>A	XP_011515027.1:p.Thr1229=
XM_011516726.1:c.2643G>A	XP_011515028.1:p.Thr881=
XM_011516727.1:c.2643G>A	XP_011515029.1:p.Thr881=
XM_011516728.1:c.2514G>A	XP_011515030.1:p.Thr838=
XM_011516729.1:c.2466G>A	XP_011515031.1:p.Thr822=
XM_011516718.2:c.3687G>A	XP_011515020.1:p.Thr1229=
XM_011516719.3:c.3327G>A	XP_011515021.1:p.Thr1109=
XM_011516720.3:c.3327G>A	XP_011515022.1:p.Thr1109=
XM_011516726.3:c.2643G>A	XP_011515028.1:p.Thr881=
XM_017012840.2:c.3816G>A	XP_016868329.1:p.Thr1272=
XM_017012841.2:c.3813G>A	XP_016868330.1:p.Thr1271=
XM_017012842.2:c.3810G>A	XP_016868331.1:p.Thr1270=
XM_017012843.2:c.3774G>A	XP_016868332.1:p.Thr1258=
XM_017012844.2:c.3816G>A	XP_016868333.1:p.Thr1272=
XM_017012845.2:c.3681G>A	XP_016868334.1:p.Thr1227=
XM_017012846.2:c.3645G>A	XP_016868335.1:p.Thr1215=
XM_017012847.2:c.3327G>A	XP_016868336.1:p.Thr1109=
XM_017012848.2:c.3198G>A	XP_016868337.1:p.Thr1066=
XM_017012849.2:c.3192G>A	XP_016868338.1:p.Thr1064=
XM_017012850.2:c.3816G>A	XP_016868339.1:p.Thr1272=
XM_017012851.2:c.3816G>A	XP_016868340.1:p.Thr1272=
XM_017012852.2:c.3816G>A	XP_016868341.1:p.Thr1272=
XM_024447009.1:c.3327G>A	XP_024302777.1:p.Thr1109=
NM_012301.4:c.3687G>A MANE Select	NP_036433.2:p.Thr1229=
NM_001301128.2:c.3645G>A	NP_001288057.1:p.Thr1215=