Canonical Allele Identifier: CA4313743

Gene: MAGI2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.78167992A>G , CM000669.2:g.78167992A>G	GRCh38
NC_000007.13:g.77797309A>G , CM000669.1:g.77797309A>G	GRCh37
NC_000007.12:g.77635245A>G	NCBI36
NG_011487.1:g.1290582T>C
NG_011487.2:g.1290583T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354212.9:c.2520T>C MANE Select	ENSP00000346151.4:p.Tyr840=
ENST00000636178.1:c.1590T>C	ENSP00000489709.1:p.Tyr530=
ENST00000637282.1:c.1299T>C	ENSP00000490637.1:p.Tyr433=
ENST00000637441.1:c.2478T>C	ENSP00000489633.1:p.Tyr826=
ENST00000637486.1:c.*622T>C	ENSP00000490080.1:n.*622T>C
ENST00000354212.8:c.2520T>C	ENSP00000346151.4:p.Tyr840=
ENST00000419488.5:c.2478T>C	ENSP00000405766.1:p.Tyr826=
ENST00000519748.5:c.1299T>C	ENSP00000486774.1:p.Tyr433=
ENST00000522342.3:c.174T>C	ENSP00000486379.1:p.Tyr58=
ENST00000522391.3:c.2520T>C	ENSP00000428389.1:p.Tyr840=
ENST00000535697.5:c.2064T>C	ENSP00000441603.3:p.Tyr688=
ENST00000626691.2:c.2031T>C	ENSP00000486131.1:p.Tyr677=
ENST00000628361.1:c.435T>C	ENSP00000486154.1:p.Tyr145=
ENST00000628980.2:c.2106T>C	ENSP00000487526.1:p.Tyr702=
ENST00000629359.2:c.1989T>C	ENSP00000487448.1:p.Tyr663=
NM_001301128.1:c.2478T>C	NP_001288057.1:p.Tyr826=
NM_012301.3:c.2520T>C	NP_036433.2:p.Tyr840=
XM_011516718.1:c.2520T>C	XP_011515020.1:p.Tyr840=
XM_011516719.1:c.2160T>C	XP_011515021.1:p.Tyr720=
XM_011516720.1:c.2160T>C	XP_011515022.1:p.Tyr720=
XM_011516721.1:c.1989T>C	XP_011515023.1:p.Tyr663=
XM_011516722.1:c.1980T>C	XP_011515024.1:p.Tyr660=
XM_011516723.1:c.2520T>C	XP_011515025.1:p.Tyr840=
XM_011516724.1:c.2520T>C	XP_011515026.1:p.Tyr840=
XM_011516725.1:c.2520T>C	XP_011515027.1:p.Tyr840=
XM_011516726.1:c.1476T>C	XP_011515028.1:p.Tyr492=
XM_011516727.1:c.1476T>C	XP_011515029.1:p.Tyr492=
XM_011516728.1:c.1347T>C	XP_011515030.1:p.Tyr449=
XM_011516729.1:c.1299T>C	XP_011515031.1:p.Tyr433=
XM_011516718.2:c.2520T>C	XP_011515020.1:p.Tyr840=
XM_011516719.3:c.2160T>C	XP_011515021.1:p.Tyr720=
XM_011516720.3:c.2160T>C	XP_011515022.1:p.Tyr720=
XM_011516726.3:c.1476T>C	XP_011515028.1:p.Tyr492=
XM_017012840.2:c.2649T>C	XP_016868329.1:p.Tyr883=
XM_017012841.2:c.2646T>C	XP_016868330.1:p.Tyr882=
XM_017012842.2:c.2643T>C	XP_016868331.1:p.Tyr881=
XM_017012843.2:c.2607T>C	XP_016868332.1:p.Tyr869=
XM_017012844.2:c.2649T>C	XP_016868333.1:p.Tyr883=
XM_017012845.2:c.2514T>C	XP_016868334.1:p.Tyr838=
XM_017012846.2:c.2478T>C	XP_016868335.1:p.Tyr826=
XM_017012847.2:c.2160T>C	XP_016868336.1:p.Tyr720=
XM_017012848.2:c.2031T>C	XP_016868337.1:p.Tyr677=
XM_017012849.2:c.2025T>C	XP_016868338.1:p.Tyr675=
XM_017012850.2:c.2649T>C	XP_016868339.1:p.Tyr883=
XM_017012851.2:c.2649T>C	XP_016868340.1:p.Tyr883=
XM_017012852.2:c.2649T>C	XP_016868341.1:p.Tyr883=
XM_024447009.1:c.2160T>C	XP_024302777.1:p.Tyr720=
NM_012301.4:c.2520T>C MANE Select	NP_036433.2:p.Tyr840=
NM_001301128.2:c.2478T>C	NP_001288057.1:p.Tyr826=