Canonical Allele Identifier: CA395677460

Gene: FUS

Linked Data

• ClinVar Variation Id: 540279
• ClinVar RCV Id: RCV000650268 ; RCV000664221
• dbSNP Id: rs1555509693
• MyVariant Identifiers: chr16:g.31202742A>G (hg19) ; chr16:g.31191421A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31191421A>G , CM000678.2:g.31191421A>G	GRCh38
NC_000016.9:g.31202742A>G , CM000678.1:g.31202742A>G	GRCh37
NC_000016.8:g.31110243A>G	NCBI36
NG_012889.2:g.16290A>G , LRG_655:g.16290A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000254108.12:c.1564A>G MANE Select	ENSP00000254108.8:p.Arg522Gly
ENST00000254108.11:c.1564A>G	ENSP00000254108.7:p.Arg522Gly
ENST00000380244.7:c.1561A>G	ENSP00000369594.3:p.Arg521Gly
ENST00000483853.1:n.641A>G
ENST00000487509.6:n.4739A>G
ENST00000566605.5:c.*737A>G	ENSP00000455073.1:n.*737A>G
ENST00000568685.1:c.1567A>G	ENSP00000455282.1:p.Arg523Gly
ENST00000569760.5:n.455A>G
NM_001170634.1:c.1561A>G	NP_001164105.1:p.Arg521Gly
NM_001170937.1:c.1552A>G	NP_001164408.1:p.Arg518Gly
NM_004960.3:c.1564A>G , LRG_655t1:c.1564A>G	NP_004951.1:p.Arg522Gly
NR_028388.2:n.1634A>G
XM_005255233.3:c.949A>G	XP_005255290.1:p.Arg317Gly
XM_011545781.1:c.1558A>G	XP_011544083.1:p.Arg520Gly
XM_011545782.1:c.949A>G	XP_011544084.1:p.Arg317Gly
XM_005255233.5:c.949A>G	XP_005255290.1:p.Arg317Gly
XM_011545782.2:c.949A>G	XP_011544084.1:p.Arg317Gly
XM_024450221.1:c.1555A>G	XP_024305989.1:p.Arg519Gly
NM_004960.4:c.1564A>G MANE Select	NP_004951.1:p.Arg522Gly