Canonical Allele Identifier: CA2439054288
Gene: MAGT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77870975G= , CM000685.2:g.77870975G= GRCh38
NC_000023.10:g.77126472G= , CM000685.1:g.77126472G= GRCh37
NC_000023.9:g.77013128G= NCBI36
NG_016390.1:g.29594C= , LRG_353:g.29594C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000358075.11:c.273-50C= ENSP00000354649.6:n.273-50C=
ENST00000685002.1:n.300-50C=
ENST00000685015.1:c.273-50C= ENSP00000509969.1:n.273-50C=
ENST00000685353.1:c.273-50C= ENSP00000510266.1:n.273-50C=
ENST00000688650.1:c.273-50C= ENSP00000509785.1:n.273-50C=
ENST00000689137.1:c.171-50C= ENSP00000509458.1:n.171-50C=
ENST00000689519.1:c.273-50C= ENSP00000509887.1:n.273-50C=
ENST00000691172.1:c.171-50C= ENSP00000508529.1:n.171-50C=
ENST00000691993.1:c.369-50C= ENSP00000509067.1:n.369-50C=
ENST00000692161.1:c.273-50C= ENSP00000509676.1:n.273-50C=
ENST00000618282.5:c.273-50C= MANE Select ENSP00000480732.1:n.273-50C=
ENST00000358075.10:c.369-50C= ENSP00000354649.5:n.369-50C=
ENST00000373336.3:c.273-50C= ENSP00000362433.3:n.273-50C=
ENST00000476168.1:n.287-50C=
ENST00000610432.4:c.369-50C= ENSP00000478379.1:n.369-50C=
ENST00000618282.4:c.273-50C= ENSP00000480732.1:n.273-50C=
NM_032121.5:c.369-50C= , LRG_353t1:c.369-50C= NP_115497.4:n.369-50C=
NM_001367916.1:c.273-50C= MANE Select NP_001354845.1:n.273-50C=