Canonical Allele Identifier: CA4313931

Gene: MAGI2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.78256076A>C , CM000669.2:g.78256076A>C	GRCh38
NC_000007.13:g.77885393A>C , CM000669.1:g.77885393A>C	GRCh37
NC_000007.12:g.77723329A>C	NCBI36
NG_011487.1:g.1202498T>G
NG_011487.2:g.1202499T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354212.9:c.1914T>G MANE Select	ENSP00000346151.4:p.Pro638=
ENST00000636039.1:c.984T>G	ENSP00000490259.1:p.Pro328=
ENST00000636178.1:c.984T>G	ENSP00000489709.1:p.Pro328=
ENST00000636717.1:c.1410T>G	ENSP00000490128.1:p.Pro470=
ENST00000637282.1:c.741T>G	ENSP00000490637.1:p.Pro247=
ENST00000637441.1:c.1914T>G	ENSP00000489633.1:p.Pro638=
ENST00000637486.1:c.*16T>G	ENSP00000490080.1:n.*16T>G
ENST00000354212.8:c.1914T>G	ENSP00000346151.4:p.Pro638=
ENST00000419488.5:c.1914T>G	ENSP00000405766.1:p.Pro638=
ENST00000519748.5:c.741T>G	ENSP00000486774.1:p.Pro247=
ENST00000520379.2:n.989T>G
ENST00000522391.3:c.1914T>G	ENSP00000428389.1:p.Pro638=
ENST00000535697.5:c.1500T>G	ENSP00000441603.3:p.Pro500=
ENST00000626691.2:c.1425T>G	ENSP00000486131.1:p.Pro475=
ENST00000628781.1:c.1425T>G	ENSP00000485970.1:p.Pro475=
ENST00000628980.2:c.1500T>G	ENSP00000487526.1:p.Pro500=
ENST00000629359.2:c.1425T>G	ENSP00000487448.1:p.Pro475=
ENST00000630991.2:c.1245T>G	ENSP00000487435.1:p.Pro415=
NM_001301128.1:c.1914T>G	NP_001288057.1:p.Pro638=
NM_012301.3:c.1914T>G	NP_036433.2:p.Pro638=
XM_011516718.1:c.1914T>G	XP_011515020.1:p.Pro638=
XM_011516719.1:c.1554T>G	XP_011515021.1:p.Pro518=
XM_011516720.1:c.1554T>G	XP_011515022.1:p.Pro518=
XM_011516721.1:c.1425T>G	XP_011515023.1:p.Pro475=
XM_011516722.1:c.1374T>G	XP_011515024.1:p.Pro458=
XM_011516723.1:c.1914T>G	XP_011515025.1:p.Pro638=
XM_011516724.1:c.1914T>G	XP_011515026.1:p.Pro638=
XM_011516725.1:c.1914T>G	XP_011515027.1:p.Pro638=
XM_011516726.1:c.870T>G	XP_011515028.1:p.Pro290=
XM_011516727.1:c.870T>G	XP_011515029.1:p.Pro290=
XM_011516728.1:c.741T>G	XP_011515030.1:p.Pro247=
XM_011516729.1:c.741T>G	XP_011515031.1:p.Pro247=
XM_011516718.2:c.1914T>G	XP_011515020.1:p.Pro638=
XM_011516719.3:c.1554T>G	XP_011515021.1:p.Pro518=
XM_011516720.3:c.1554T>G	XP_011515022.1:p.Pro518=
XM_011516726.3:c.870T>G	XP_011515028.1:p.Pro290=
XM_017012840.2:c.2043T>G	XP_016868329.1:p.Pro681=
XM_017012841.2:c.2040T>G	XP_016868330.1:p.Pro680=
XM_017012842.2:c.2043T>G	XP_016868331.1:p.Pro681=
XM_017012843.2:c.2043T>G	XP_016868332.1:p.Pro681=
XM_017012844.2:c.2043T>G	XP_016868333.1:p.Pro681=
XM_017012845.2:c.1914T>G	XP_016868334.1:p.Pro638=
XM_017012846.2:c.1914T>G	XP_016868335.1:p.Pro638=
XM_017012847.2:c.1554T>G	XP_016868336.1:p.Pro518=
XM_017012848.2:c.1425T>G	XP_016868337.1:p.Pro475=
XM_017012849.2:c.1425T>G	XP_016868338.1:p.Pro475=
XM_017012850.2:c.2043T>G	XP_016868339.1:p.Pro681=
XM_017012851.2:c.2043T>G	XP_016868340.1:p.Pro681=
XM_017012852.2:c.2043T>G	XP_016868341.1:p.Pro681=
XM_024447009.1:c.1554T>G	XP_024302777.1:p.Pro518=
NM_012301.4:c.1914T>G MANE Select	NP_036433.2:p.Pro638=
NM_001301128.2:c.1914T>G	NP_001288057.1:p.Pro638=