Canonical Allele Identifier: CA1719353399

Gene: MAGI2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.78529132T= , CM000669.2:g.78529132T=	GRCh38
NC_000007.13:g.78158449T= , CM000669.1:g.78158449T=	GRCh37
NC_000007.12:g.77996385T=	NCBI36
NG_011487.1:g.929442A=
NG_011487.2:g.929443A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354212.9:c.539-7487A= MANE Select	ENSP00000346151.4:n.539-7487A=
ENST00000635863.1:n.327-7487A=
ENST00000636717.1:c.35-7487A=	ENSP00000490128.1:n.35-7487A=
ENST00000637441.1:c.539-7487A=	ENSP00000489633.1:n.539-7487A=
ENST00000637486.1:c.50-7487A=	ENSP00000490080.1:n.50-7487A=
ENST00000637728.1:n.251-7487A=
ENST00000354212.8:c.539-7487A=	ENSP00000346151.4:n.539-7487A=
ENST00000419488.5:c.539-7487A=	ENSP00000405766.1:n.539-7487A=
ENST00000517762.2:n.3-7487A=
ENST00000522391.3:c.539-7487A=	ENSP00000428389.1:n.539-7487A=
ENST00000535697.5:c.125-7487A=	ENSP00000441603.3:n.125-7487A=
ENST00000626691.2:c.50-7487A=	ENSP00000486131.1:n.50-7487A=
ENST00000628781.1:c.50-7487A=	ENSP00000485970.1:n.50-7487A=
ENST00000628980.2:c.125-7487A=	ENSP00000487526.1:n.125-7487A=
ENST00000629359.2:c.50-7487A=	ENSP00000487448.1:n.50-7487A=
ENST00000630991.2:c.-131-7487A=	ENSP00000487435.1:n.-131-7487A=
NM_001301128.1:c.539-7487A=	NP_001288057.1:n.539-7487A=
NM_012301.3:c.539-7487A=	NP_036433.2:n.539-7487A=
XM_011516718.1:c.539-7487A=	XP_011515020.1:n.539-7487A=
XM_011516719.1:c.50-7487A=	XP_011515021.1:n.50-7487A=
XM_011516720.1:c.50-7487A=	XP_011515022.1:n.50-7487A=
XM_011516721.1:c.50-7487A=	XP_011515023.1:n.50-7487A=
XM_011516722.1:c.-131-7487A=	XP_011515024.1:n.-131-7487A=
XM_011516723.1:c.539-7487A=	XP_011515025.1:n.539-7487A=
XM_011516724.1:c.539-7487A=	XP_011515026.1:n.539-7487A=
XM_011516725.1:c.539-7487A=	XP_011515027.1:n.539-7487A=
XM_011516718.2:c.539-7487A=	XP_011515020.1:n.539-7487A=
XM_011516719.3:c.50-7487A=	XP_011515021.1:n.50-7487A=
XM_011516720.3:c.50-7487A=	XP_011515022.1:n.50-7487A=
XM_017012840.2:c.539-7487A=	XP_016868329.1:n.539-7487A=
XM_017012841.2:c.539-7487A=	XP_016868330.1:n.539-7487A=
XM_017012842.2:c.539-7487A=	XP_016868331.1:n.539-7487A=
XM_017012843.2:c.539-7487A=	XP_016868332.1:n.539-7487A=
XM_017012844.2:c.539-7487A=	XP_016868333.1:n.539-7487A=
XM_017012845.2:c.539-7487A=	XP_016868334.1:n.539-7487A=
XM_017012846.2:c.539-7487A=	XP_016868335.1:n.539-7487A=
XM_017012847.2:c.50-7487A=	XP_016868336.1:n.50-7487A=
XM_017012848.2:c.50-7487A=	XP_016868337.1:n.50-7487A=
XM_017012849.2:c.50-7487A=	XP_016868338.1:n.50-7487A=
XM_017012850.2:c.539-7487A=	XP_016868339.1:n.539-7487A=
XM_017012851.2:c.539-7487A=	XP_016868340.1:n.539-7487A=
XM_017012852.2:c.539-7487A=	XP_016868341.1:n.539-7487A=
XM_024447009.1:c.50-7487A=	XP_024302777.1:n.50-7487A=
NM_012301.4:c.539-7487A= MANE Select	NP_036433.2:n.539-7487A=
NM_001301128.2:c.539-7487A=	NP_001288057.1:n.539-7487A=