Canonical Allele Identifier: CA1719128525

Gene: MAGI2

Linked Data

• dbSNP Id: rs1810889692

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.78041933C>A , CM000669.2:g.78041933C>A	GRCh38
NC_000007.13:g.77671250C>A , CM000669.1:g.77671250C>A	GRCh37
NC_000007.12:g.77509186C>A	NCBI36
NG_011487.1:g.1416641G>T
NG_011487.2:g.1416642G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354212.9:c.3707-21957G>T MANE Select	ENSP00000346151.4:n.3707-21957G>T
ENST00000635961.1:n.83-6726G>T
ENST00000637441.1:c.3479-21957G>T	ENSP00000489633.1:n.3479-21957G>T
ENST00000637585.1:c.79-15829G>T	ENSP00000490629.1:n.79-15829G>T
ENST00000637976.1:n.28-2302G>T
ENST00000354212.8:c.3707-21957G>T	ENSP00000346151.4:n.3707-21957G>T
ENST00000419488.5:c.3665-21957G>T	ENSP00000405766.1:n.3665-21957G>T
ENST00000522391.3:c.3796-21957G>T	ENSP00000428389.1:n.3796-21957G>T
ENST00000535697.5:c.3251-21957G>T	ENSP00000441603.3:n.3251-21957G>T
ENST00000626691.2:c.3307-21957G>T	ENSP00000486131.1:n.3307-21957G>T
ENST00000628980.2:c.3293-21957G>T	ENSP00000487526.1:n.3293-21957G>T
ENST00000629359.2:c.3265-21957G>T	ENSP00000487448.1:n.3265-21957G>T
NM_001301128.1:c.3665-21957G>T	NP_001288057.1:n.3665-21957G>T
NM_012301.3:c.3707-21957G>T	NP_036433.2:n.3707-21957G>T
XM_011516718.1:c.3796-15829G>T	XP_011515020.1:n.3796-15829G>T
XM_011516719.1:c.3436-15829G>T	XP_011515021.1:n.3436-15829G>T
XM_011516720.1:c.3436-15829G>T	XP_011515022.1:n.3436-15829G>T
XM_011516721.1:c.3265-15829G>T	XP_011515023.1:n.3265-15829G>T
XM_011516722.1:c.3256-15829G>T	XP_011515024.1:n.3256-15829G>T
XM_011516723.1:c.3796-21957G>T	XP_011515025.1:n.3796-21957G>T
XM_011516724.1:c.*50-21957G>T	XP_011515026.1:n.*50-21957G>T
XM_011516725.1:c.*50-15829G>T	XP_011515027.1:n.*50-15829G>T
XM_011516726.1:c.2752-15829G>T	XP_011515028.1:n.2752-15829G>T
XM_011516727.1:c.2752-15829G>T	XP_011515029.1:n.2752-15829G>T
XM_011516728.1:c.2623-15829G>T	XP_011515030.1:n.2623-15829G>T
XM_011516729.1:c.2575-15829G>T	XP_011515031.1:n.2575-15829G>T
XM_011516718.2:c.3796-15829G>T	XP_011515020.1:n.3796-15829G>T
XM_011516719.3:c.3436-15829G>T	XP_011515021.1:n.3436-15829G>T
XM_011516720.3:c.3436-15829G>T	XP_011515022.1:n.3436-15829G>T
XM_011516726.3:c.2752-15829G>T	XP_011515028.1:n.2752-15829G>T
XM_017012840.2:c.3925-15829G>T	XP_016868329.1:n.3925-15829G>T
XM_017012841.2:c.3922-15829G>T	XP_016868330.1:n.3922-15829G>T
XM_017012842.2:c.3919-15829G>T	XP_016868331.1:n.3919-15829G>T
XM_017012843.2:c.3883-15829G>T	XP_016868332.1:n.3883-15829G>T
XM_017012844.2:c.3836-21957G>T	XP_016868333.1:n.3836-21957G>T
XM_017012845.2:c.3790-15829G>T	XP_016868334.1:n.3790-15829G>T
XM_017012846.2:c.3754-15829G>T	XP_016868335.1:n.3754-15829G>T
XM_017012847.2:c.3436-15829G>T	XP_016868336.1:n.3436-15829G>T
XM_017012848.2:c.3307-15829G>T	XP_016868337.1:n.3307-15829G>T
XM_017012849.2:c.3301-15829G>T	XP_016868338.1:n.3301-15829G>T
XM_017012850.2:c.3925-21957G>T	XP_016868339.1:n.3925-21957G>T
XM_017012851.2:c.*50-21957G>T	XP_016868340.1:n.*50-21957G>T
XM_017012852.2:c.3836-15829G>T	XP_016868341.1:n.3836-15829G>T
XM_024447009.1:c.3436-15829G>T	XP_024302777.1:n.3436-15829G>T
NM_012301.4:c.3707-21957G>T MANE Select	NP_036433.2:n.3707-21957G>T
NM_001301128.2:c.3665-21957G>T	NP_001288057.1:n.3665-21957G>T