Canonical Allele Identifier: CA413710993

Gene: MAGT1

Linked Data

• COSMIC: COSM6410142 ; COSM6410143
• MyVariant Identifiers: chrX:g.77126308C>A (hg19) ; chrX:g.77870811C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77870811C>A , CM000685.2:g.77870811C>A	GRCh38
NC_000023.10:g.77126308C>A , CM000685.1:g.77126308C>A	GRCh37
NC_000023.9:g.77012964C>A	NCBI36
NG_016390.1:g.29758G>T , LRG_353:g.29758G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358075.11:c.387G>T	ENSP00000354649.6:p.Gln129His
ENST00000685002.1:n.414G>T
ENST00000685015.1:c.387G>T	ENSP00000509969.1:p.Gln129His
ENST00000685353.1:c.387G>T	ENSP00000510266.1:p.Gln129His
ENST00000688650.1:c.387G>T	ENSP00000509785.1:p.Gln129His
ENST00000689137.1:c.285G>T	ENSP00000509458.1:p.Gln95His
ENST00000689519.1:c.387G>T	ENSP00000509887.1:p.Gln129His
ENST00000691172.1:c.285G>T	ENSP00000508529.1:p.Gln95His
ENST00000691993.1:c.483G>T	ENSP00000509067.1:p.Gln161His
ENST00000692161.1:c.387G>T	ENSP00000509676.1:p.Gln129His
ENST00000618282.5:c.387G>T MANE Select	ENSP00000480732.1:p.Gln129His
ENST00000358075.10:c.483G>T	ENSP00000354649.5:p.Gln161His
ENST00000373336.3:c.387G>T	ENSP00000362433.3:p.Gln129His
ENST00000476168.1:n.401G>T
ENST00000610432.4:c.483G>T	ENSP00000478379.1:p.Gln161His
ENST00000618282.4:c.387G>T	ENSP00000480732.1:p.Gln129His
NM_032121.5:c.483G>T , LRG_353t1:c.483G>T	NP_115497.4:p.Gln161His
NM_001367916.1:c.387G>T MANE Select	NP_001354845.1:p.Gln129His