Canonical Allele Identifier: CA2579649883

Gene: MAGT1

Linked Data

• gnomAD v4: X-77870786-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77870786C>T , CM000685.2:g.77870786C>T	GRCh38
NC_000023.10:g.77126283C>T , CM000685.1:g.77126283C>T	GRCh37
NC_000023.9:g.77012939C>T	NCBI36
NG_016390.1:g.29783G>A , LRG_353:g.29783G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358075.11:c.390+22G>A	ENSP00000354649.6:n.390+22G>A
ENST00000685002.1:n.417+22G>A
ENST00000685015.1:c.390+22G>A	ENSP00000509969.1:n.390+22G>A
ENST00000685353.1:c.390+22G>A	ENSP00000510266.1:n.390+22G>A
ENST00000688650.1:c.390+22G>A	ENSP00000509785.1:n.390+22G>A
ENST00000689137.1:c.288+22G>A	ENSP00000509458.1:n.288+22G>A
ENST00000689519.1:c.390+22G>A	ENSP00000509887.1:n.390+22G>A
ENST00000691172.1:c.288+22G>A	ENSP00000508529.1:n.288+22G>A
ENST00000691993.1:c.486+22G>A	ENSP00000509067.1:n.486+22G>A
ENST00000692161.1:c.390+22G>A	ENSP00000509676.1:n.390+22G>A
ENST00000618282.5:c.390+22G>A MANE Select	ENSP00000480732.1:n.390+22G>A
ENST00000358075.10:c.486+22G>A	ENSP00000354649.5:n.486+22G>A
ENST00000373336.3:c.390+22G>A	ENSP00000362433.3:n.390+22G>A
ENST00000476168.1:n.404+22G>A
ENST00000610432.4:c.486+22G>A	ENSP00000478379.1:n.486+22G>A
ENST00000618282.4:c.390+22G>A	ENSP00000480732.1:n.390+22G>A
NM_032121.5:c.486+22G>A , LRG_353t1:c.486+22G>A	NP_115497.4:n.486+22G>A
NM_001367916.1:c.390+22G>A MANE Select	NP_001354845.1:n.390+22G>A