Canonical Allele Identifier: CA2756597916

Gene: MAGI1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.65393544del , CM000665.2:g.65393544del	GRCh38
NC_000003.11:g.65379219del , CM000665.1:g.65379219del	GRCh37
NC_000003.10:g.65354259del	NCBI36
NG_029778.1:g.650297del
NG_029778.2:g.650297del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402939.7:c.2200-2180del MANE Select	ENSP00000385450.2:n.2200-2180del
ENST00000330909.12:c.2200-2180del	ENSP00000331157.7:n.2200-2180del
ENST00000402939.6:c.2200-2180del	ENSP00000385450.2:n.2200-2180del
ENST00000460329.6:c.1842-2180del
ENST00000463103.6:c.1825-2180del	ENSP00000418177.2:n.1825-2180del
ENST00000468159.1:n.176-2180del
ENST00000472257.5:c.1558-2180del	ENSP00000420796.1:n.1558-2180del
ENST00000483466.5:c.2200-2180del	ENSP00000420323.1:n.2200-2180del
ENST00000497477.6:c.2200-2180del	ENSP00000424369.1:n.2200-2180del
ENST00000611645.4:c.1279-2180del	ENSP00000480920.1:n.1279-2180del
ENST00000621418.4:c.1279-2180del	ENSP00000477591.1:n.1279-2180del
NM_001033057.1:c.2200-2180del	NP_001028229.1:n.2200-2180del
NM_004742.2:c.2200-2180del	NP_004733.2:n.2200-2180del
NM_015520.1:c.2200-2180del	NP_056335.1:n.2200-2180del
XM_005265563.1:c.2206-2180del	XP_005265620.1:n.2206-2180del
XM_005265564.1:c.2200-2180del	XP_005265621.1:n.2200-2180del
XM_005265565.1:c.2206-2180del	XP_005265622.1:n.2206-2180del
XM_005265566.1:c.2200-2180del	XP_005265623.1:n.2200-2180del
XM_005265568.1:c.2164-2180del	XP_005265625.1:n.2164-2180del
XM_005265570.1:c.2206-2180del	XP_005265627.1:n.2206-2180del
XM_005265571.1:c.2200-2180del	XP_005265628.1:n.2200-2180del
XM_005265574.2:c.2200-2180del	XP_005265631.1:n.2200-2180del
XM_006713407.1:c.2206-2180del	XP_006713470.1:n.2206-2180del
XM_006713408.1:c.2203-2180del	XP_006713471.1:n.2203-2180del
XM_006713409.1:c.2203-2180del	XP_006713472.1:n.2203-2180del
XM_006713410.1:c.2164-2180del	XP_006713473.1:n.2164-2180del
XM_006713411.1:c.2206-2180del	XP_006713474.1:n.2206-2180del
XM_006713412.1:c.2200-2180del	XP_006713475.1:n.2200-2180del
XM_006713413.2:c.1804-2180del	XP_006713476.2:n.1804-2180del
XM_006713414.2:c.2206-2180del	XP_006713477.1:n.2206-2180del
XM_011534236.1:c.2167-2180del	XP_011532538.1:n.2167-2180del
XM_011534237.1:c.2131-2180del	XP_011532539.1:n.2131-2180del
XM_011534238.1:c.1522-2180del	XP_011532540.1:n.1522-2180del
XM_011534239.1:c.2206-2180del	XP_011532541.1:n.2206-2180del
XM_011534240.1:c.49-2180del	XP_011532542.1:n.49-2180del
XM_011534241.1:c.49-2180del	XP_011532543.1:n.49-2180del
NM_001365903.1:c.2203-2180del	NP_001352832.1:n.2203-2180del
NM_001365904.1:c.2203-2180del	NP_001352833.1:n.2203-2180del
NM_001365905.1:c.2203-2180del	NP_001352834.1:n.2203-2180del
NM_001033057.2:c.2200-2180del MANE Select	NP_001028229.1:n.2200-2180del
NM_001365903.2:c.2203-2180del	NP_001352832.1:n.2203-2180del
NM_001365904.2:c.2203-2180del	NP_001352833.1:n.2203-2180del
NM_004742.3:c.2200-2180del	NP_004733.2:n.2200-2180del
NM_015520.2:c.2200-2180del	NP_056335.1:n.2200-2180del