Canonical Allele Identifier: CA4313529

Gene: MAGI2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.78127241G>T , CM000669.2:g.78127241G>T	GRCh38
NC_000007.13:g.77756558G>T , CM000669.1:g.77756558G>T	GRCh37
NC_000007.12:g.77594494G>T	NCBI36
NG_011487.1:g.1331333C>A
NG_011487.2:g.1331334C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_012301.4:c.3379C>A MANE Select	NP_036433.2:p.Pro1127Thr
ENST00000354212.9:c.3379C>A MANE Select	ENSP00000346151.4:p.Pro1127Thr
NM_001301128.1:c.3337C>A	NP_001288057.1:p.Pro1113Thr
NM_001301128.2:c.3337C>A	NP_001288057.1:p.Pro1113Thr
NM_012301.3:c.3379C>A	NP_036433.2:p.Pro1127Thr
ENST00000354212.8:c.3379C>A	ENSP00000346151.4:p.Pro1127Thr
ENST00000419488.5:c.3337C>A	ENSP00000405766.1:p.Pro1113Thr
ENST00000519748.5:c.2158C>A	ENSP00000486774.1:p.Pro720Thr
ENST00000522391.3:c.3379C>A	ENSP00000428389.1:p.Pro1127Thr
ENST00000535697.5:c.2923C>A	ENSP00000441603.3:p.Pro975Thr
ENST00000626691.2:c.2890C>A	ENSP00000486131.1:p.Pro964Thr
ENST00000628980.2:c.2965C>A	ENSP00000487526.1:p.Pro989Thr
ENST00000629359.2:c.2848C>A	ENSP00000487448.1:p.Pro950Thr
ENST00000637282.1:c.2158C>A	ENSP00000490637.1:p.Pro720Thr
ENST00000637441.1:c.3151C>A	ENSP00000489633.1:p.Pro1051Thr
ENST00000637486.1:c.*1481C>A	ENSP00000490080.1:n.*1481C>A
XM_011516718.1:c.3379C>A	XP_011515020.1:p.Pro1127Thr
XM_011516718.2:c.3379C>A	XP_011515020.1:p.Pro1127Thr
XM_011516719.1:c.3019C>A	XP_011515021.1:p.Pro1007Thr
XM_011516719.3:c.3019C>A	XP_011515021.1:p.Pro1007Thr
XM_011516720.1:c.3019C>A	XP_011515022.1:p.Pro1007Thr
XM_011516720.3:c.3019C>A	XP_011515022.1:p.Pro1007Thr
XM_011516721.1:c.2848C>A	XP_011515023.1:p.Pro950Thr
XM_011516722.1:c.2839C>A	XP_011515024.1:p.Pro947Thr
XM_011516723.1:c.3379C>A	XP_011515025.1:p.Pro1127Thr
XM_011516724.1:c.3379C>A	XP_011515026.1:p.Pro1127Thr
XM_011516725.1:c.3379C>A	XP_011515027.1:p.Pro1127Thr
XM_011516726.1:c.2335C>A	XP_011515028.1:p.Pro779Thr
XM_011516726.3:c.2335C>A	XP_011515028.1:p.Pro779Thr
XM_011516727.1:c.2335C>A	XP_011515029.1:p.Pro779Thr
XM_011516728.1:c.2206C>A	XP_011515030.1:p.Pro736Thr
XM_011516729.1:c.2158C>A	XP_011515031.1:p.Pro720Thr
XM_017012840.2:c.3508C>A	XP_016868329.1:p.Pro1170Thr
XM_017012841.2:c.3505C>A	XP_016868330.1:p.Pro1169Thr
XM_017012842.2:c.3502C>A	XP_016868331.1:p.Pro1168Thr
XM_017012843.2:c.3466C>A	XP_016868332.1:p.Pro1156Thr
XM_017012844.2:c.3508C>A	XP_016868333.1:p.Pro1170Thr
XM_017012845.2:c.3373C>A	XP_016868334.1:p.Pro1125Thr
XM_017012846.2:c.3337C>A	XP_016868335.1:p.Pro1113Thr
XM_017012847.2:c.3019C>A	XP_016868336.1:p.Pro1007Thr
XM_017012848.2:c.2890C>A	XP_016868337.1:p.Pro964Thr
XM_017012849.2:c.2884C>A	XP_016868338.1:p.Pro962Thr
XM_017012850.2:c.3508C>A	XP_016868339.1:p.Pro1170Thr
XM_017012851.2:c.3508C>A	XP_016868340.1:p.Pro1170Thr
XM_017012852.2:c.3508C>A	XP_016868341.1:p.Pro1170Thr
XM_024447009.1:c.3019C>A	XP_024302777.1:p.Pro1007Thr