Canonical Allele Identifier: CA2439054262
Gene: MAGT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77870898C= , CM000685.2:g.77870898C= GRCh38
NC_000023.10:g.77126395C= , CM000685.1:g.77126395C= GRCh37
NC_000023.9:g.77013051C= NCBI36
NG_016390.1:g.29671G= , LRG_353:g.29671G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000358075.11:c.300G= ENSP00000354649.6:p.Leu100=
ENST00000685002.1:n.327G=
ENST00000685015.1:c.300G= ENSP00000509969.1:p.Leu100=
ENST00000685353.1:c.300G= ENSP00000510266.1:p.Leu100=
ENST00000688650.1:c.300G= ENSP00000509785.1:p.Leu100=
ENST00000689137.1:c.198G= ENSP00000509458.1:p.Leu66=
ENST00000689519.1:c.300G= ENSP00000509887.1:p.Leu100=
ENST00000691172.1:c.198G= ENSP00000508529.1:p.Leu66=
ENST00000691993.1:c.396G= ENSP00000509067.1:p.Leu132=
ENST00000692161.1:c.300G= ENSP00000509676.1:p.Leu100=
ENST00000618282.5:c.300G= MANE Select ENSP00000480732.1:p.Leu100=
ENST00000358075.10:c.396G= ENSP00000354649.5:p.Leu132=
ENST00000373336.3:c.300G= ENSP00000362433.3:p.Leu100=
ENST00000476168.1:n.314G=
ENST00000610432.4:c.396G= ENSP00000478379.1:p.Leu132=
ENST00000618282.4:c.300G= ENSP00000480732.1:p.Leu100=
NM_032121.5:c.396G= , LRG_353t1:c.396G= NP_115497.4:p.Leu132=
NM_001367916.1:c.300G= MANE Select NP_001354845.1:p.Leu100=