Canonical Allele Identifier: CA413711426

Gene: MAGT1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77841252G>A , CM000685.2:g.77841252G>A	GRCh38
NC_000023.10:g.77096749G>A , CM000685.1:g.77096749G>A	GRCh37
NC_000023.9:g.76983405G>A	NCBI36
NG_016390.1:g.59317C>T , LRG_353:g.59317C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001367916.1:c.895C>T MANE Select	NP_001354845.1:p.Arg299Ter
ENST00000618282.5:c.895C>T MANE Select	ENSP00000480732.1:p.Arg299Ter
NM_032121.5:c.991C>T , LRG_353t1:c.991C>T	NP_115497.4:p.Arg331Ter
ENST00000358075.10:c.991C>T	ENSP00000354649.5:p.Arg331Ter
ENST00000358075.11:c.895C>T	ENSP00000354649.6:p.Arg299Ter
ENST00000610432.4:c.991C>T	ENSP00000478379.1:p.Arg331Ter
ENST00000618282.4:c.895C>T	ENSP00000480732.1:p.Arg299Ter
ENST00000685015.1:c.895C>T	ENSP00000509969.1:p.Arg299Ter
ENST00000685353.1:c.805C>T	ENSP00000510266.1:p.Arg269Ter
ENST00000688650.1:c.805C>T	ENSP00000509785.1:p.Arg269Ter
ENST00000689137.1:c.793C>T	ENSP00000509458.1:p.Arg265Ter
ENST00000689519.1:c.895C>T	ENSP00000509887.1:p.Arg299Ter
ENST00000691172.1:c.793C>T	ENSP00000508529.1:p.Arg265Ter
ENST00000691993.1:c.991C>T	ENSP00000509067.1:p.Arg331Ter
ENST00000692161.1:c.613C>T	ENSP00000509676.1:p.Arg205Ter