Canonical Allele Identifier: CA16621510

Gene: MAGT1

Linked Data

• ClinVar Variation Id: 419298
• ClinVar RCV Id: RCV000479226 ; RCV000850121
• dbSNP Id: rs200934080
• MyVariant Identifiers: chrX:g.77150894C>T (hg19) ; chrX:g.77895397C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77895397C>T , CM000685.2:g.77895397C>T	GRCh38
NC_000023.10:g.77150894C>T , CM000685.1:g.77150894C>T	GRCh37
NC_000023.9:g.77037550C>T	NCBI36
NG_016390.1:g.5172G>A , LRG_353:g.5172G>A
NG_033027.1:g.934C>T
NG_033027.2:g.934C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358075.11:c.14G>A	ENSP00000354649.6:p.Trp5Ter
ENST00000685002.1:n.41G>A
ENST00000685015.1:c.14G>A	ENSP00000509969.1:p.Trp5Ter
ENST00000685353.1:c.14G>A	ENSP00000510266.1:p.Trp5Ter
ENST00000688650.1:c.14G>A	ENSP00000509785.1:p.Trp5Ter
ENST00000689137.1:c.-1+3783G>A	ENSP00000509458.1:n.-1+3783G>A
ENST00000689519.1:c.14G>A	ENSP00000509887.1:p.Trp5Ter
ENST00000691172.1:c.-230G>A	ENSP00000508529.1:n.-230G>A
ENST00000691993.1:c.110G>A	ENSP00000509067.1:p.Trp37Ter
ENST00000692161.1:c.14G>A	ENSP00000509676.1:p.Trp5Ter
ENST00000618282.5:c.14G>A MANE Select	ENSP00000480732.1:p.Trp5Ter
ENST00000358075.10:c.110G>A	ENSP00000354649.5:p.Trp37Ter
ENST00000373336.3:c.14G>A	ENSP00000362433.3:p.Trp5Ter
ENST00000476168.1:n.28G>A
ENST00000610432.4:c.110G>A	ENSP00000478379.1:p.Trp37Ter
ENST00000618282.4:c.14G>A	ENSP00000480732.1:p.Trp5Ter
NM_032121.5:c.110G>A , LRG_353t1:c.110G>A	NP_115497.4:p.Trp37Ter
NM_001367916.1:c.14G>A MANE Select	NP_001354845.1:p.Trp5Ter