Canonical Allele Identifier: CA1189841754

Gene: MAGI3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113630863T= , CM000663.2:g.113630863T=	GRCh38
NC_000001.10:g.114173485T= , CM000663.1:g.114173485T=	GRCh37
NC_000001.9:g.113975008T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307546.14:c.1360+7869T= MANE Select	ENSP00000304604.9:n.1360+7869T=
ENST00000307546.13:c.1360+7869T=	ENSP00000304604.9:n.1360+7869T=
ENST00000369611.4:c.1360+7869T=	ENSP00000358624.4:n.1360+7869T=
ENST00000369615.5:c.1360+7869T=	ENSP00000358628.1:n.1360+7869T=
ENST00000369617.8:c.1435+7869T=	ENSP00000358630.4:n.1435+7869T=
NM_001142782.1:c.1360+7869T=	NP_001136254.1:n.1360+7869T=
NM_152900.2:c.1360+7869T=	NP_690864.2:n.1360+7869T=
XM_005270737.2:c.1360+7869T=	XP_005270794.1:n.1360+7869T=
XM_011541208.1:c.676+7869T=	XP_011539510.1:n.676+7869T=
XR_946601.1:n.1920+7869T=
XM_005270737.3:c.1360+7869T=	XP_005270794.1:n.1360+7869T=
XM_011541208.2:c.676+7869T=	XP_011539510.1:n.676+7869T=
XM_017000974.1:c.1360+7869T=	XP_016856463.1:n.1360+7869T=
XM_017000975.1:c.187+7869T=	XP_016856464.1:n.187+7869T=
XR_001737106.1:n.1920+7869T=
XR_946601.2:n.1920+7869T=
NM_001142782.2:c.1360+7869T= MANE Select	NP_001136254.1:n.1360+7869T=
NM_152900.3:c.1360+7869T=	NP_690864.2:n.1360+7869T=