Canonical Allele Identifier: CA11593768

Gene: MAGI1

Linked Data

• dbSNP Id: rs1524976
• gnomAD v2: 3-65486388-A-G
• gnomAD v3: 3-65500713-A-G
• gnomAD v4: 3-65500713-A-G
• MyVariant Identifiers: chr3:g.65486388A>G (hg19) ; chr3:g.65500713A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.65500713A>G , CM000665.2:g.65500713A>G	GRCh38
NC_000003.11:g.65486388A>G , CM000665.1:g.65486388A>G	GRCh37
NC_000003.10:g.65461428A>G	NCBI36
NG_029778.1:g.543122T>C
NG_029778.2:g.543122T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000402939.7:c.431-7082T>C MANE Select	ENSP00000385450.2:n.431-7082T>C
ENST00000330909.12:c.431-7082T>C	ENSP00000331157.7:n.431-7082T>C
ENST00000402939.6:c.431-7082T>C	ENSP00000385450.2:n.431-7082T>C
ENST00000460329.6:c.73-7082T>C
ENST00000463103.6:c.56-7082T>C	ENSP00000418177.2:n.56-7082T>C
ENST00000464060.5:n.957-7082T>C
ENST00000470990.5:n.955-7082T>C
ENST00000476403.5:n.94-7082T>C
ENST00000483466.5:c.431-7082T>C	ENSP00000420323.1:n.431-7082T>C
ENST00000496734.1:n.145-7082T>C
ENST00000497477.6:c.431-7082T>C	ENSP00000424369.1:n.431-7082T>C
ENST00000611645.4:c.-491-7082T>C	ENSP00000480920.1:n.-491-7082T>C
ENST00000621418.4:c.-491-7082T>C	ENSP00000477591.1:n.-491-7082T>C
NM_001033057.1:c.431-7082T>C	NP_001028229.1:n.431-7082T>C
NM_004742.2:c.431-7082T>C	NP_004733.2:n.431-7082T>C
NM_015520.1:c.431-7082T>C	NP_056335.1:n.431-7082T>C
XM_005265563.1:c.431-7082T>C	XP_005265620.1:n.431-7082T>C
XM_005265564.1:c.431-7082T>C	XP_005265621.1:n.431-7082T>C
XM_005265565.1:c.431-7082T>C	XP_005265622.1:n.431-7082T>C
XM_005265566.1:c.431-7082T>C	XP_005265623.1:n.431-7082T>C
XM_005265568.1:c.431-7082T>C	XP_005265625.1:n.431-7082T>C
XM_005265570.1:c.431-7082T>C	XP_005265627.1:n.431-7082T>C
XM_005265571.1:c.431-7082T>C	XP_005265628.1:n.431-7082T>C
XM_005265574.2:c.431-7082T>C	XP_005265631.1:n.431-7082T>C
XM_006713407.1:c.431-7082T>C	XP_006713470.1:n.431-7082T>C
XM_006713408.1:c.431-7082T>C	XP_006713471.1:n.431-7082T>C
XM_006713409.1:c.431-7082T>C	XP_006713472.1:n.431-7082T>C
XM_006713410.1:c.431-7082T>C	XP_006713473.1:n.431-7082T>C
XM_006713411.1:c.431-7082T>C	XP_006713474.1:n.431-7082T>C
XM_006713412.1:c.431-7082T>C	XP_006713475.1:n.431-7082T>C
XM_006713413.2:c.29-7082T>C	XP_006713476.2:n.29-7082T>C
XM_006713414.2:c.431-7082T>C	XP_006713477.1:n.431-7082T>C
XM_011534236.1:c.431-7082T>C	XP_011532538.1:n.431-7082T>C
XM_011534237.1:c.356-7082T>C	XP_011532539.1:n.356-7082T>C
XM_011534239.1:c.431-7082T>C	XP_011532541.1:n.431-7082T>C
NM_001365903.1:c.431-7082T>C	NP_001352832.1:n.431-7082T>C
NM_001365904.1:c.431-7082T>C	NP_001352833.1:n.431-7082T>C
NM_001365905.1:c.431-7082T>C	NP_001352834.1:n.431-7082T>C
NM_001033057.2:c.431-7082T>C MANE Select	NP_001028229.1:n.431-7082T>C
NM_001365903.2:c.431-7082T>C	NP_001352832.1:n.431-7082T>C
NM_001365904.2:c.431-7082T>C	NP_001352833.1:n.431-7082T>C
NM_004742.3:c.431-7082T>C	NP_004733.2:n.431-7082T>C
NM_015520.2:c.431-7082T>C	NP_056335.1:n.431-7082T>C