Canonical Allele Identifier: CA2579649892
Gene: MAGT1 HGNC NCBI

Linked Data

gnomAD v4: X-77870968-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77870968T>C , CM000685.2:g.77870968T>C GRCh38
NC_000023.10:g.77126465T>C , CM000685.1:g.77126465T>C GRCh37
NC_000023.9:g.77013121T>C NCBI36
NG_016390.1:g.29601A>G , LRG_353:g.29601A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000358075.11:c.273-43A>G ENSP00000354649.6:n.273-43A>G
ENST00000685002.1:n.300-43A>G
ENST00000685015.1:c.273-43A>G ENSP00000509969.1:n.273-43A>G
ENST00000685353.1:c.273-43A>G ENSP00000510266.1:n.273-43A>G
ENST00000688650.1:c.273-43A>G ENSP00000509785.1:n.273-43A>G
ENST00000689137.1:c.171-43A>G ENSP00000509458.1:n.171-43A>G
ENST00000689519.1:c.273-43A>G ENSP00000509887.1:n.273-43A>G
ENST00000691172.1:c.171-43A>G ENSP00000508529.1:n.171-43A>G
ENST00000691993.1:c.369-43A>G ENSP00000509067.1:n.369-43A>G
ENST00000692161.1:c.273-43A>G ENSP00000509676.1:n.273-43A>G
ENST00000618282.5:c.273-43A>G MANE Select ENSP00000480732.1:n.273-43A>G
ENST00000358075.10:c.369-43A>G ENSP00000354649.5:n.369-43A>G
ENST00000373336.3:c.273-43A>G ENSP00000362433.3:n.273-43A>G
ENST00000476168.1:n.287-43A>G
ENST00000610432.4:c.369-43A>G ENSP00000478379.1:n.369-43A>G
ENST00000618282.4:c.273-43A>G ENSP00000480732.1:n.273-43A>G
NM_032121.5:c.369-43A>G , LRG_353t1:c.369-43A>G NP_115497.4:n.369-43A>G
NM_001367916.1:c.273-43A>G MANE Select NP_001354845.1:n.273-43A>G