Canonical Allele Identifier: CA517376564

Gene: MAGT1

Linked Data

• ClinVar Variation Id: 2791120
• ClinVar RCV Id: RCV003641242
• MyVariant Identifiers: chrX:g.77126416A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77870919A>G , CM000685.2:g.77870919A>G	GRCh38
NC_000023.10:g.77126416A>G , CM000685.1:g.77126416A>G	GRCh37
NC_000023.9:g.77013072A>G	NCBI36
NG_016390.1:g.29650T>C , LRG_353:g.29650T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358075.11:c.279T>C	ENSP00000354649.6:p.Ala93=
ENST00000685002.1:n.306T>C
ENST00000685015.1:c.279T>C	ENSP00000509969.1:p.Ala93=
ENST00000685353.1:c.279T>C	ENSP00000510266.1:p.Ala93=
ENST00000688650.1:c.279T>C	ENSP00000509785.1:p.Ala93=
ENST00000689137.1:c.177T>C	ENSP00000509458.1:p.Ala59=
ENST00000689519.1:c.279T>C	ENSP00000509887.1:p.Ala93=
ENST00000691172.1:c.177T>C	ENSP00000508529.1:p.Ala59=
ENST00000691993.1:c.375T>C	ENSP00000509067.1:p.Ala125=
ENST00000692161.1:c.279T>C	ENSP00000509676.1:p.Ala93=
ENST00000618282.5:c.279T>C MANE Select	ENSP00000480732.1:p.Ala93=
ENST00000358075.10:c.375T>C	ENSP00000354649.5:p.Ala125=
ENST00000373336.3:c.279T>C	ENSP00000362433.3:p.Ala93=
ENST00000476168.1:n.293T>C
ENST00000610432.4:c.375T>C	ENSP00000478379.1:p.Ala125=
ENST00000618282.4:c.279T>C	ENSP00000480732.1:p.Ala93=
NM_032121.5:c.375T>C , LRG_353t1:c.375T>C	NP_115497.4:p.Ala125=
NM_001367916.1:c.279T>C MANE Select	NP_001354845.1:p.Ala93=