Canonical Allele Identifier: CA413713680

Gene: MAGT1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77856777T>C , CM000685.2:g.77856777T>C	GRCh38
NC_000023.10:g.77112274T>C , CM000685.1:g.77112274T>C	GRCh37
NC_000023.9:g.76998930T>C	NCBI36
NG_016390.1:g.43792A>G , LRG_353:g.43792A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001367916.1:c.628A>G MANE Select	NP_001354845.1:p.Met210Val
ENST00000618282.5:c.628A>G MANE Select	ENSP00000480732.1:p.Met210Val
NM_032121.5:c.724A>G , LRG_353t1:c.724A>G	NP_115497.4:p.Met242Val
ENST00000358075.10:c.724A>G	ENSP00000354649.5:p.Met242Val
ENST00000358075.11:c.628A>G	ENSP00000354649.6:p.Met210Val
ENST00000476168.1:n.642A>G
ENST00000610432.4:c.724A>G	ENSP00000478379.1:p.Met242Val
ENST00000618282.4:c.628A>G	ENSP00000480732.1:p.Met210Val
ENST00000685002.1:n.655A>G
ENST00000685015.1:c.628A>G	ENSP00000509969.1:p.Met210Val
ENST00000685353.1:c.628A>G	ENSP00000510266.1:p.Met210Val
ENST00000688650.1:c.628A>G	ENSP00000509785.1:p.Met210Val
ENST00000689137.1:c.526A>G	ENSP00000509458.1:p.Met176Val
ENST00000689519.1:c.628A>G	ENSP00000509887.1:p.Met210Val
ENST00000691172.1:c.526A>G	ENSP00000508529.1:p.Met176Val
ENST00000691993.1:c.724A>G	ENSP00000509067.1:p.Met242Val
ENST00000692161.1:c.391-1187A>G	ENSP00000509676.1:n.391-1187A>G