Canonical Allele Identifier: CA148581

Gene: MAGI2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.78019414C>G , CM000669.2:g.78019414C>G	GRCh38
NC_000007.13:g.77648731C>G , CM000669.1:g.77648731C>G	GRCh37
NC_000007.12:g.77486667C>G	NCBI36
NG_011487.1:g.1439160G>C
NG_011487.2:g.1439161G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354212.9:c.4269G>C MANE Select	ENSP00000346151.4:p.Pro1423=
ENST00000637441.1:c.3532-199G>C	ENSP00000489633.1:n.3532-199G>C
ENST00000354212.8:c.4269G>C	ENSP00000346151.4:p.Pro1423=
ENST00000419488.5:c.4227G>C	ENSP00000405766.1:p.Pro1409=
ENST00000522391.3:c.*506G>C	ENSP00000428389.1:n.*506G>C
ENST00000535697.5:c.3813G>C	ENSP00000441603.3:p.Pro1271=
ENST00000626691.2:c.*506G>C	ENSP00000486131.1:n.*506G>C
ENST00000628980.2:c.3855G>C	ENSP00000487526.1:p.Pro1285=
ENST00000629359.2:c.*506G>C	ENSP00000487448.1:n.*506G>C
NM_001301128.1:c.4227G>C	NP_001288057.1:p.Pro1409=
NM_012301.3:c.4269G>C	NP_036433.2:p.Pro1423=
XM_011516718.1:c.4395G>C	XP_011515020.1:p.Pro1465=
XM_011516719.1:c.4035G>C	XP_011515021.1:p.Pro1345=
XM_011516720.1:c.4035G>C	XP_011515022.1:p.Pro1345=
XM_011516721.1:c.3864G>C	XP_011515023.1:p.Pro1288=
XM_011516722.1:c.3855G>C	XP_011515024.1:p.Pro1285=
XM_011516726.1:c.3351G>C	XP_011515028.1:p.Pro1117=
XM_011516727.1:c.3351G>C	XP_011515029.1:p.Pro1117=
XM_011516728.1:c.3222G>C	XP_011515030.1:p.Pro1074=
XM_011516729.1:c.3174G>C	XP_011515031.1:p.Pro1058=
XM_011516718.2:c.4395G>C	XP_011515020.1:p.Pro1465=
XM_011516719.3:c.4035G>C	XP_011515021.1:p.Pro1345=
XM_011516720.3:c.4035G>C	XP_011515022.1:p.Pro1345=
XM_011516726.3:c.3351G>C	XP_011515028.1:p.Pro1117=
XM_017012840.2:c.4524G>C	XP_016868329.1:p.Pro1508=
XM_017012841.2:c.4521G>C	XP_016868330.1:p.Pro1507=
XM_017012842.2:c.4518G>C	XP_016868331.1:p.Pro1506=
XM_017012843.2:c.4482G>C	XP_016868332.1:p.Pro1494=
XM_017012844.2:c.4398G>C	XP_016868333.1:p.Pro1466=
XM_017012845.2:c.4389G>C	XP_016868334.1:p.Pro1463=
XM_017012846.2:c.4353G>C	XP_016868335.1:p.Pro1451=
XM_017012847.2:c.4035G>C	XP_016868336.1:p.Pro1345=
XM_017012848.2:c.3906G>C	XP_016868337.1:p.Pro1302=
XM_017012849.2:c.3900G>C	XP_016868338.1:p.Pro1300=
XM_024447009.1:c.4035G>C	XP_024302777.1:p.Pro1345=
NM_012301.4:c.4269G>C MANE Select	NP_036433.2:p.Pro1423=
NM_001301128.2:c.4227G>C	NP_001288057.1:p.Pro1409=