Canonical Allele Identifier: CA4313748

Gene: MAGI2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.78168010G>A , CM000669.2:g.78168010G>A	GRCh38
NC_000007.13:g.77797327G>A , CM000669.1:g.77797327G>A	GRCh37
NC_000007.12:g.77635263G>A	NCBI36
NG_011487.1:g.1290564C>T
NG_011487.2:g.1290565C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354212.9:c.2502C>T MANE Select	ENSP00000346151.4:p.Ala834=
ENST00000636178.1:c.1572C>T	ENSP00000489709.1:p.Ala524=
ENST00000637282.1:c.1281C>T	ENSP00000490637.1:p.Ala427=
ENST00000637441.1:c.2460C>T	ENSP00000489633.1:p.Ala820=
ENST00000637486.1:c.*604C>T	ENSP00000490080.1:n.*604C>T
ENST00000354212.8:c.2502C>T	ENSP00000346151.4:p.Ala834=
ENST00000419488.5:c.2460C>T	ENSP00000405766.1:p.Ala820=
ENST00000519748.5:c.1281C>T	ENSP00000486774.1:p.Ala427=
ENST00000522342.3:c.156C>T	ENSP00000486379.1:p.Ala52=
ENST00000522391.3:c.2502C>T	ENSP00000428389.1:p.Ala834=
ENST00000535697.5:c.2046C>T	ENSP00000441603.3:p.Ala682=
ENST00000626691.2:c.2013C>T	ENSP00000486131.1:p.Ala671=
ENST00000628361.1:c.417C>T	ENSP00000486154.1:p.Ala139=
ENST00000628980.2:c.2088C>T	ENSP00000487526.1:p.Ala696=
ENST00000629359.2:c.1971C>T	ENSP00000487448.1:p.Ala657=
NM_001301128.1:c.2460C>T	NP_001288057.1:p.Ala820=
NM_012301.3:c.2502C>T	NP_036433.2:p.Ala834=
XM_011516718.1:c.2502C>T	XP_011515020.1:p.Ala834=
XM_011516719.1:c.2142C>T	XP_011515021.1:p.Ala714=
XM_011516720.1:c.2142C>T	XP_011515022.1:p.Ala714=
XM_011516721.1:c.1971C>T	XP_011515023.1:p.Ala657=
XM_011516722.1:c.1962C>T	XP_011515024.1:p.Ala654=
XM_011516723.1:c.2502C>T	XP_011515025.1:p.Ala834=
XM_011516724.1:c.2502C>T	XP_011515026.1:p.Ala834=
XM_011516725.1:c.2502C>T	XP_011515027.1:p.Ala834=
XM_011516726.1:c.1458C>T	XP_011515028.1:p.Ala486=
XM_011516727.1:c.1458C>T	XP_011515029.1:p.Ala486=
XM_011516728.1:c.1329C>T	XP_011515030.1:p.Ala443=
XM_011516729.1:c.1281C>T	XP_011515031.1:p.Ala427=
XM_011516718.2:c.2502C>T	XP_011515020.1:p.Ala834=
XM_011516719.3:c.2142C>T	XP_011515021.1:p.Ala714=
XM_011516720.3:c.2142C>T	XP_011515022.1:p.Ala714=
XM_011516726.3:c.1458C>T	XP_011515028.1:p.Ala486=
XM_017012840.2:c.2631C>T	XP_016868329.1:p.Ala877=
XM_017012841.2:c.2628C>T	XP_016868330.1:p.Ala876=
XM_017012842.2:c.2625C>T	XP_016868331.1:p.Ala875=
XM_017012843.2:c.2589C>T	XP_016868332.1:p.Ala863=
XM_017012844.2:c.2631C>T	XP_016868333.1:p.Ala877=
XM_017012845.2:c.2496C>T	XP_016868334.1:p.Ala832=
XM_017012846.2:c.2460C>T	XP_016868335.1:p.Ala820=
XM_017012847.2:c.2142C>T	XP_016868336.1:p.Ala714=
XM_017012848.2:c.2013C>T	XP_016868337.1:p.Ala671=
XM_017012849.2:c.2007C>T	XP_016868338.1:p.Ala669=
XM_017012850.2:c.2631C>T	XP_016868339.1:p.Ala877=
XM_017012851.2:c.2631C>T	XP_016868340.1:p.Ala877=
XM_017012852.2:c.2631C>T	XP_016868341.1:p.Ala877=
XM_024447009.1:c.2142C>T	XP_024302777.1:p.Ala714=
NM_012301.4:c.2502C>T MANE Select	NP_036433.2:p.Ala834=
NM_001301128.2:c.2460C>T	NP_001288057.1:p.Ala820=