Canonical Allele Identifier: CA161236956

Gene: MAGI2

Linked Data

• dbSNP Id: rs945736162
• MyVariant Identifiers: chr7:g.78043309G>A (hg19) ; chr7:g.78413992G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.78413992G>A , CM000669.2:g.78413992G>A	GRCh38
NC_000007.13:g.78043309G>A , CM000669.1:g.78043309G>A	GRCh37
NC_000007.12:g.77881245G>A	NCBI36
NG_011487.1:g.1044582C>T
NG_011487.2:g.1044583C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354212.9:c.1046-44779C>T MANE Select	ENSP00000346151.4:n.1046-44779C>T
ENST00000636039.1:c.116-44779C>T	ENSP00000490259.1:n.116-44779C>T
ENST00000636178.1:c.116-44779C>T	ENSP00000489709.1:n.116-44779C>T
ENST00000636717.1:c.542-44779C>T	ENSP00000490128.1:n.542-44779C>T
ENST00000637074.1:n.32-44779C>T
ENST00000637282.1:c.-128-44779C>T	ENSP00000490637.1:n.-128-44779C>T
ENST00000637441.1:c.1046-44779C>T	ENSP00000489633.1:n.1046-44779C>T
ENST00000637486.1:c.557-44779C>T	ENSP00000490080.1:n.557-44779C>T
ENST00000354212.8:c.1046-44779C>T	ENSP00000346151.4:n.1046-44779C>T
ENST00000419488.5:c.1046-44779C>T	ENSP00000405766.1:n.1046-44779C>T
ENST00000519748.5:c.-128-44779C>T	ENSP00000486774.1:n.-128-44779C>T
ENST00000520379.2:n.121-44779C>T
ENST00000522391.3:c.1046-44779C>T	ENSP00000428389.1:n.1046-44779C>T
ENST00000535697.5:c.632-44779C>T	ENSP00000441603.3:n.632-44779C>T
ENST00000626691.2:c.557-44779C>T	ENSP00000486131.1:n.557-44779C>T
ENST00000628781.1:c.557-44779C>T	ENSP00000485970.1:n.557-44779C>T
ENST00000628980.2:c.632-44779C>T	ENSP00000487526.1:n.632-44779C>T
ENST00000629359.2:c.557-44779C>T	ENSP00000487448.1:n.557-44779C>T
ENST00000630991.2:c.377-44779C>T	ENSP00000487435.1:n.377-44779C>T
ENST00000634996.1:c.-128-44779C>T	ENSP00000489533.1:n.-128-44779C>T
NM_001301128.1:c.1046-44779C>T	NP_001288057.1:n.1046-44779C>T
NM_012301.3:c.1046-44779C>T	NP_036433.2:n.1046-44779C>T
XM_011516718.1:c.1046-44779C>T	XP_011515020.1:n.1046-44779C>T
XM_011516719.1:c.557-44779C>T	XP_011515021.1:n.557-44779C>T
XM_011516720.1:c.557-44779C>T	XP_011515022.1:n.557-44779C>T
XM_011516721.1:c.557-44779C>T	XP_011515023.1:n.557-44779C>T
XM_011516722.1:c.377-44779C>T	XP_011515024.1:n.377-44779C>T
XM_011516723.1:c.1046-44779C>T	XP_011515025.1:n.1046-44779C>T
XM_011516724.1:c.1046-44779C>T	XP_011515026.1:n.1046-44779C>T
XM_011516725.1:c.1046-44779C>T	XP_011515027.1:n.1046-44779C>T
XM_011516726.1:c.-128-44779C>T	XP_011515028.1:n.-128-44779C>T
XM_011516727.1:c.-129+34950C>T	XP_011515029.1:n.-129+34950C>T
XM_011516728.1:c.-128-44779C>T	XP_011515030.1:n.-128-44779C>T
XM_011516729.1:c.-128-44779C>T	XP_011515031.1:n.-128-44779C>T
XM_011516718.2:c.1046-44779C>T	XP_011515020.1:n.1046-44779C>T
XM_011516719.3:c.557-44779C>T	XP_011515021.1:n.557-44779C>T
XM_011516720.3:c.557-44779C>T	XP_011515022.1:n.557-44779C>T
XM_011516726.3:c.-128-44779C>T	XP_011515028.1:n.-128-44779C>T
XM_017012840.2:c.1046-44779C>T	XP_016868329.1:n.1046-44779C>T
XM_017012841.2:c.1046-44779C>T	XP_016868330.1:n.1046-44779C>T
XM_017012842.2:c.1046-44779C>T	XP_016868331.1:n.1046-44779C>T
XM_017012843.2:c.1046-44779C>T	XP_016868332.1:n.1046-44779C>T
XM_017012844.2:c.1046-44779C>T	XP_016868333.1:n.1046-44779C>T
XM_017012845.2:c.1046-44779C>T	XP_016868334.1:n.1046-44779C>T
XM_017012846.2:c.1046-44779C>T	XP_016868335.1:n.1046-44779C>T
XM_017012847.2:c.557-44779C>T	XP_016868336.1:n.557-44779C>T
XM_017012848.2:c.557-44779C>T	XP_016868337.1:n.557-44779C>T
XM_017012849.2:c.557-44779C>T	XP_016868338.1:n.557-44779C>T
XM_017012850.2:c.1046-44779C>T	XP_016868339.1:n.1046-44779C>T
XM_017012851.2:c.1046-44779C>T	XP_016868340.1:n.1046-44779C>T
XM_017012852.2:c.1046-44779C>T	XP_016868341.1:n.1046-44779C>T
XM_024447009.1:c.557-44779C>T	XP_024302777.1:n.557-44779C>T
NM_012301.4:c.1046-44779C>T MANE Select	NP_036433.2:n.1046-44779C>T
NM_001301128.2:c.1046-44779C>T	NP_001288057.1:n.1046-44779C>T