Canonical Allele Identifier: CA642702715

Gene: MAGT1

Linked Data

• dbSNP Id: rs1174169488
• gnomAD v2: X-77126434-G-C
• gnomAD v3: X-77870937-G-C
• gnomAD v4: X-77870937-G-C
• MyVariant Identifiers: chrX:g.77126434G>C (hg19) ; chrX:g.77870937G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77870937G>C , CM000685.2:g.77870937G>C	GRCh38
NC_000023.10:g.77126434G>C , CM000685.1:g.77126434G>C	GRCh37
NC_000023.9:g.77013090G>C	NCBI36
NG_016390.1:g.29632C>G , LRG_353:g.29632C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358075.11:c.273-12C>G	ENSP00000354649.6:n.273-12C>G
ENST00000685002.1:n.300-12C>G
ENST00000685015.1:c.273-12C>G	ENSP00000509969.1:n.273-12C>G
ENST00000685353.1:c.273-12C>G	ENSP00000510266.1:n.273-12C>G
ENST00000688650.1:c.273-12C>G	ENSP00000509785.1:n.273-12C>G
ENST00000689137.1:c.171-12C>G	ENSP00000509458.1:n.171-12C>G
ENST00000689519.1:c.273-12C>G	ENSP00000509887.1:n.273-12C>G
ENST00000691172.1:c.171-12C>G	ENSP00000508529.1:n.171-12C>G
ENST00000691993.1:c.369-12C>G	ENSP00000509067.1:n.369-12C>G
ENST00000692161.1:c.273-12C>G	ENSP00000509676.1:n.273-12C>G
ENST00000618282.5:c.273-12C>G MANE Select	ENSP00000480732.1:n.273-12C>G
ENST00000358075.10:c.369-12C>G	ENSP00000354649.5:n.369-12C>G
ENST00000373336.3:c.273-12C>G	ENSP00000362433.3:n.273-12C>G
ENST00000476168.1:n.287-12C>G
ENST00000610432.4:c.369-12C>G	ENSP00000478379.1:n.369-12C>G
ENST00000618282.4:c.273-12C>G	ENSP00000480732.1:n.273-12C>G
NM_032121.5:c.369-12C>G , LRG_353t1:c.369-12C>G	NP_115497.4:n.369-12C>G
NM_001367916.1:c.273-12C>G MANE Select	NP_001354845.1:n.273-12C>G