Canonical Allele Identifier: CA413711291

Gene: MAGT1

Linked Data

• MyVariant Identifiers: chrX:g.77126387G>A (hg19) ; chrX:g.77870890G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77870890G>A , CM000685.2:g.77870890G>A	GRCh38
NC_000023.10:g.77126387G>A , CM000685.1:g.77126387G>A	GRCh37
NC_000023.9:g.77013043G>A	NCBI36
NG_016390.1:g.29679C>T , LRG_353:g.29679C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358075.11:c.308C>T	ENSP00000354649.6:p.Ser103Phe
ENST00000685002.1:n.335C>T
ENST00000685015.1:c.308C>T	ENSP00000509969.1:p.Ser103Phe
ENST00000685353.1:c.308C>T	ENSP00000510266.1:p.Ser103Phe
ENST00000688650.1:c.308C>T	ENSP00000509785.1:p.Ser103Phe
ENST00000689137.1:c.206C>T	ENSP00000509458.1:p.Ser69Phe
ENST00000689519.1:c.308C>T	ENSP00000509887.1:p.Ser103Phe
ENST00000691172.1:c.206C>T	ENSP00000508529.1:p.Ser69Phe
ENST00000691993.1:c.404C>T	ENSP00000509067.1:p.Ser135Phe
ENST00000692161.1:c.308C>T	ENSP00000509676.1:p.Ser103Phe
ENST00000618282.5:c.308C>T MANE Select	ENSP00000480732.1:p.Ser103Phe
ENST00000358075.10:c.404C>T	ENSP00000354649.5:p.Ser135Phe
ENST00000373336.3:c.308C>T	ENSP00000362433.3:p.Ser103Phe
ENST00000476168.1:n.322C>T
ENST00000610432.4:c.404C>T	ENSP00000478379.1:p.Ser135Phe
ENST00000618282.4:c.308C>T	ENSP00000480732.1:p.Ser103Phe
NM_032121.5:c.404C>T , LRG_353t1:c.404C>T	NP_115497.4:p.Ser135Phe
NM_001367916.1:c.308C>T MANE Select	NP_001354845.1:p.Ser103Phe