Canonical Allele Identifier: CA413714123

Gene: MAGT1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77857398C>A , CM000685.2:g.77857398C>A	GRCh38
NC_000023.10:g.77112895C>A , CM000685.1:g.77112895C>A	GRCh37
NC_000023.9:g.76999551C>A	NCBI36
NG_016390.1:g.43171G>T , LRG_353:g.43171G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358075.11:c.490G>T	ENSP00000354649.6:p.Glu164Ter
ENST00000685002.1:n.517G>T
ENST00000685015.1:c.490G>T	ENSP00000509969.1:p.Glu164Ter
ENST00000685353.1:c.490G>T	ENSP00000510266.1:p.Glu164Ter
ENST00000688650.1:c.490G>T	ENSP00000509785.1:p.Glu164Ter
ENST00000689137.1:c.388G>T	ENSP00000509458.1:p.Glu130Ter
ENST00000689519.1:c.490G>T	ENSP00000509887.1:p.Glu164Ter
ENST00000691172.1:c.388G>T	ENSP00000508529.1:p.Glu130Ter
ENST00000691993.1:c.586G>T	ENSP00000509067.1:p.Glu196Ter
ENST00000692161.1:c.391-1808G>T	ENSP00000509676.1:n.391-1808G>T
ENST00000618282.5:c.490G>T MANE Select	ENSP00000480732.1:p.Glu164Ter
ENST00000358075.10:c.586G>T	ENSP00000354649.5:p.Glu196Ter
ENST00000476168.1:n.504G>T
ENST00000610432.4:c.586G>T	ENSP00000478379.1:p.Glu196Ter
ENST00000618282.4:c.490G>T	ENSP00000480732.1:p.Glu164Ter
NM_032121.5:c.586G>T , LRG_353t1:c.586G>T	NP_115497.4:p.Glu196Ter
NM_001367916.1:c.490G>T MANE Select	NP_001354845.1:p.Glu164Ter