Canonical Allele Identifier: CA10458618

Gene: MAGT1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77895413T>C , CM000685.2:g.77895413T>C	GRCh38
NC_000023.10:g.77150910T>C , CM000685.1:g.77150910T>C	GRCh37
NC_000023.9:g.77037566T>C	NCBI36
NG_016390.1:g.5156A>G , LRG_353:g.5156A>G
NG_033027.1:g.950T>C
NG_033027.2:g.950T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001367916.1:c.-3A>G MANE Select	NP_001354845.1:n.-3A>G
ENST00000618282.5:c.-3A>G MANE Select	ENSP00000480732.1:n.-3A>G
NM_032121.5:c.94A>G , LRG_353t1:c.94A>G	NP_115497.4:p.Asn32Asp
ENST00000358075.10:c.94A>G	ENSP00000354649.5:p.Asn32Asp
ENST00000358075.11:c.-3A>G	ENSP00000354649.6:n.-3A>G
ENST00000373336.3:c.-3A>G	ENSP00000362433.3:n.-3A>G
ENST00000476168.1:n.12A>G
ENST00000610432.4:c.94A>G	ENSP00000478379.1:p.Asn32Asp
ENST00000618282.4:c.-3A>G	ENSP00000480732.1:n.-3A>G
ENST00000685002.1:n.25A>G
ENST00000685015.1:c.-3A>G	ENSP00000509969.1:n.-3A>G
ENST00000685353.1:c.-3A>G	ENSP00000510266.1:n.-3A>G
ENST00000688650.1:c.-3A>G	ENSP00000509785.1:n.-3A>G
ENST00000689137.1:c.-1+3767A>G	ENSP00000509458.1:n.-1+3767A>G
ENST00000689519.1:c.-3A>G	ENSP00000509887.1:n.-3A>G
ENST00000691172.1:c.-246A>G	ENSP00000508529.1:n.-246A>G
ENST00000691993.1:c.94A>G	ENSP00000509067.1:p.Asn32Asp
ENST00000692161.1:c.-3A>G	ENSP00000509676.1:n.-3A>G