Canonical Allele Identifier: CA456335979

Gene: MAGI2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.78019378C>T , CM000669.2:g.78019378C>T	GRCh38
NC_000007.13:g.77648695C>T , CM000669.1:g.77648695C>T	GRCh37
NC_000007.12:g.77486631C>T	NCBI36
NG_011487.1:g.1439196G>A
NG_011487.2:g.1439197G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354212.9:c.4305G>A MANE Select	ENSP00000346151.4:p.Lys1435=
ENST00000637441.1:c.3532-163G>A	ENSP00000489633.1:n.3532-163G>A
ENST00000354212.8:c.4305G>A	ENSP00000346151.4:p.Lys1435=
ENST00000419488.5:c.4263G>A	ENSP00000405766.1:p.Lys1421=
ENST00000522391.3:c.*542G>A	ENSP00000428389.1:n.*542G>A
ENST00000535697.5:c.3849G>A	ENSP00000441603.3:p.Lys1283=
ENST00000626691.2:c.*542G>A	ENSP00000486131.1:n.*542G>A
ENST00000628980.2:c.3891G>A	ENSP00000487526.1:p.Lys1297=
ENST00000629359.2:c.*542G>A	ENSP00000487448.1:n.*542G>A
NM_001301128.1:c.4263G>A	NP_001288057.1:p.Lys1421=
NM_012301.3:c.4305G>A	NP_036433.2:p.Lys1435=
XM_011516718.1:c.4431G>A	XP_011515020.1:p.Lys1477=
XM_011516719.1:c.4071G>A	XP_011515021.1:p.Lys1357=
XM_011516720.1:c.4071G>A	XP_011515022.1:p.Lys1357=
XM_011516721.1:c.3900G>A	XP_011515023.1:p.Lys1300=
XM_011516722.1:c.3891G>A	XP_011515024.1:p.Lys1297=
XM_011516726.1:c.3387G>A	XP_011515028.1:p.Lys1129=
XM_011516727.1:c.3387G>A	XP_011515029.1:p.Lys1129=
XM_011516728.1:c.3258G>A	XP_011515030.1:p.Lys1086=
XM_011516729.1:c.3210G>A	XP_011515031.1:p.Lys1070=
XM_011516718.2:c.4431G>A	XP_011515020.1:p.Lys1477=
XM_011516719.3:c.4071G>A	XP_011515021.1:p.Lys1357=
XM_011516720.3:c.4071G>A	XP_011515022.1:p.Lys1357=
XM_011516726.3:c.3387G>A	XP_011515028.1:p.Lys1129=
XM_017012840.2:c.4560G>A	XP_016868329.1:p.Lys1520=
XM_017012841.2:c.4557G>A	XP_016868330.1:p.Lys1519=
XM_017012842.2:c.4554G>A	XP_016868331.1:p.Lys1518=
XM_017012843.2:c.4518G>A	XP_016868332.1:p.Lys1506=
XM_017012844.2:c.4434G>A	XP_016868333.1:p.Lys1478=
XM_017012845.2:c.4425G>A	XP_016868334.1:p.Lys1475=
XM_017012846.2:c.4389G>A	XP_016868335.1:p.Lys1463=
XM_017012847.2:c.4071G>A	XP_016868336.1:p.Lys1357=
XM_017012848.2:c.3942G>A	XP_016868337.1:p.Lys1314=
XM_017012849.2:c.3936G>A	XP_016868338.1:p.Lys1312=
XM_024447009.1:c.4071G>A	XP_024302777.1:p.Lys1357=
NM_012301.4:c.4305G>A MANE Select	NP_036433.2:p.Lys1435=
NM_001301128.2:c.4263G>A	NP_001288057.1:p.Lys1421=