Canonical Allele Identifier: CA10458480
Community Standard Title: NM_001367916.1(MAGT1):c.673-16T>C
Gene: MAGT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77855606A>G , CM000685.2:g.77855606A>G GRCh38
NC_000023.10:g.77111103A>G , CM000685.1:g.77111103A>G GRCh37
NC_000023.9:g.76997759A>G NCBI36
NG_016390.1:g.44963T>C , LRG_353:g.44963T>C

Transcript Alleles

HGVS Amino-acid Change
NM_001367916.1:c.673-16T>C MANE Select NP_001354845.1:n.673-16T>C
ENST00000618282.5:c.673-16T>C MANE Select ENSP00000480732.1:n.673-16T>C
NM_032121.5:c.769-16T>C , LRG_353t1:c.769-16T>C NP_115497.4:n.769-16T>C
ENST00000358075.10:c.769-16T>C ENSP00000354649.5:n.769-16T>C
ENST00000358075.11:c.673-16T>C ENSP00000354649.6:n.673-16T>C
ENST00000610432.4:c.769-16T>C ENSP00000478379.1:n.769-16T>C
ENST00000618282.4:c.673-16T>C ENSP00000480732.1:n.673-16T>C
ENST00000685002.1:n.700-16T>C
ENST00000685015.1:c.673-16T>C ENSP00000509969.1:n.673-16T>C
ENST00000685353.1:c.672+1127T>C ENSP00000510266.1:n.672+1127T>C
ENST00000688650.1:c.672+1127T>C ENSP00000509785.1:n.672+1127T>C
ENST00000689137.1:c.571-16T>C ENSP00000509458.1:n.571-16T>C
ENST00000689519.1:c.673-16T>C ENSP00000509887.1:n.673-16T>C
ENST00000691172.1:c.571-16T>C ENSP00000508529.1:n.571-16T>C
ENST00000691993.1:c.769-16T>C ENSP00000509067.1:n.769-16T>C
ENST00000692161.1:c.391-16T>C ENSP00000509676.1:n.391-16T>C