Canonical Allele Identifier: CA517376541
Gene: MAGT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.77126386G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77870889G>C , CM000685.2:g.77870889G>C GRCh38
NC_000023.10:g.77126386G>C , CM000685.1:g.77126386G>C GRCh37
NC_000023.9:g.77013042G>C NCBI36
NG_016390.1:g.29680C>G , LRG_353:g.29680C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000358075.11:c.309C>G ENSP00000354649.6:p.Ser103=
ENST00000685002.1:n.336C>G
ENST00000685015.1:c.309C>G ENSP00000509969.1:p.Ser103=
ENST00000685353.1:c.309C>G ENSP00000510266.1:p.Ser103=
ENST00000688650.1:c.309C>G ENSP00000509785.1:p.Ser103=
ENST00000689137.1:c.207C>G ENSP00000509458.1:p.Ser69=
ENST00000689519.1:c.309C>G ENSP00000509887.1:p.Ser103=
ENST00000691172.1:c.207C>G ENSP00000508529.1:p.Ser69=
ENST00000691993.1:c.405C>G ENSP00000509067.1:p.Ser135=
ENST00000692161.1:c.309C>G ENSP00000509676.1:p.Ser103=
ENST00000618282.5:c.309C>G MANE Select ENSP00000480732.1:p.Ser103=
ENST00000358075.10:c.405C>G ENSP00000354649.5:p.Ser135=
ENST00000373336.3:c.309C>G ENSP00000362433.3:p.Ser103=
ENST00000476168.1:n.323C>G
ENST00000610432.4:c.405C>G ENSP00000478379.1:p.Ser135=
ENST00000618282.4:c.309C>G ENSP00000480732.1:p.Ser103=
NM_032121.5:c.405C>G , LRG_353t1:c.405C>G NP_115497.4:p.Ser135=
NM_001367916.1:c.309C>G MANE Select NP_001354845.1:p.Ser103=