Canonical Allele Identifier: CA413711142
Gene: MAGT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77870850A>C , CM000685.2:g.77870850A>C GRCh38
NC_000023.10:g.77126347A>C , CM000685.1:g.77126347A>C GRCh37
NC_000023.9:g.77013003A>C NCBI36
NG_016390.1:g.29719T>G , LRG_353:g.29719T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000358075.11:c.348T>G ENSP00000354649.6:p.Phe116Leu
ENST00000685002.1:n.375T>G
ENST00000685015.1:c.348T>G ENSP00000509969.1:p.Phe116Leu
ENST00000685353.1:c.348T>G ENSP00000510266.1:p.Phe116Leu
ENST00000688650.1:c.348T>G ENSP00000509785.1:p.Phe116Leu
ENST00000689137.1:c.246T>G ENSP00000509458.1:p.Phe82Leu
ENST00000689519.1:c.348T>G ENSP00000509887.1:p.Phe116Leu
ENST00000691172.1:c.246T>G ENSP00000508529.1:p.Phe82Leu
ENST00000691993.1:c.444T>G ENSP00000509067.1:p.Phe148Leu
ENST00000692161.1:c.348T>G ENSP00000509676.1:p.Phe116Leu
ENST00000618282.5:c.348T>G MANE Select ENSP00000480732.1:p.Phe116Leu
ENST00000358075.10:c.444T>G ENSP00000354649.5:p.Phe148Leu
ENST00000373336.3:c.348T>G ENSP00000362433.3:p.Phe116Leu
ENST00000476168.1:n.362T>G
ENST00000610432.4:c.444T>G ENSP00000478379.1:p.Phe148Leu
ENST00000618282.4:c.348T>G ENSP00000480732.1:p.Phe116Leu
NM_032121.5:c.444T>G , LRG_353t1:c.444T>G NP_115497.4:p.Phe148Leu
NM_001367916.1:c.348T>G MANE Select NP_001354845.1:p.Phe116Leu