Canonical Allele Identifier: CA148577

Gene: MAGI2 MAGI2-AS3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.79453045G>C , CM000669.2:g.79453045G>C	GRCh38
NC_000007.13:g.79082361G>C , CM000669.1:g.79082361G>C	GRCh37
NC_000007.12:g.78920297G>C	NCBI36
NG_011487.1:g.5530C>G
NG_011487.2:g.5530C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354212.9:c.276C>G (MAGI2) MANE Select	ENSP00000346151.4:p.Pro92=
ENST00000637441.1:c.276C>G (MAGI2)	ENSP00000489633.1:p.Pro92=
ENST00000354212.8:c.276C>G (MAGI2)	ENSP00000346151.4:p.Pro92=
ENST00000419488.5:c.276C>G (MAGI2)	ENSP00000405766.1:p.Pro92=
ENST00000522391.3:c.276C>G (MAGI2)	ENSP00000428389.1:p.Pro92=
ENST00000628997.1:n.76C>G (MAGI2)
NM_001301128.1:c.276C>G (MAGI2)	NP_001288057.1:p.Pro92=
NM_012301.3:c.276C>G (MAGI2)	NP_036433.2:p.Pro92=
NR_038345.1:n.89G>C (MAGI2-AS3)
NR_038346.1:n.89G>C (MAGI2-AS3)
XM_011516718.1:c.276C>G (MAGI2)	XP_011515020.1:p.Pro92=
XM_011516723.1:c.276C>G (MAGI2)	XP_011515025.1:p.Pro92=
XM_011516724.1:c.276C>G (MAGI2)	XP_011515026.1:p.Pro92=
XM_011516725.1:c.276C>G (MAGI2)	XP_011515027.1:p.Pro92=
XM_011516718.2:c.276C>G (MAGI2)	XP_011515020.1:p.Pro92=
XM_017012840.2:c.276C>G (MAGI2)	XP_016868329.1:p.Pro92=
XM_017012841.2:c.276C>G (MAGI2)	XP_016868330.1:p.Pro92=
XM_017012842.2:c.276C>G (MAGI2)	XP_016868331.1:p.Pro92=
XM_017012843.2:c.276C>G (MAGI2)	XP_016868332.1:p.Pro92=
XM_017012844.2:c.276C>G (MAGI2)	XP_016868333.1:p.Pro92=
XM_017012845.2:c.276C>G (MAGI2)	XP_016868334.1:p.Pro92=
XM_017012846.2:c.276C>G (MAGI2)	XP_016868335.1:p.Pro92=
XM_017012850.2:c.276C>G (MAGI2)	XP_016868339.1:p.Pro92=
XM_017012851.2:c.276C>G (MAGI2)	XP_016868340.1:p.Pro92=
XM_017012852.2:c.276C>G (MAGI2)	XP_016868341.1:p.Pro92=
NM_012301.4:c.276C>G (MAGI2) MANE Select	NP_036433.2:p.Pro92=
NM_001301128.2:c.276C>G (MAGI2)	NP_001288057.1:p.Pro92=