Canonical Allele Identifier: CA395677463

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31202742A>T (hg19) ; chr16:g.31191421A>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000254108.12:c.1564A>T MANE Select	ENSP00000254108.8:p.Arg522Trp
ENST00000254108.11:c.1564A>T	ENSP00000254108.7:p.Arg522Trp
ENST00000380244.7:c.1561A>T	ENSP00000369594.3:p.Arg521Trp
ENST00000483853.1:n.641A>T
ENST00000487509.6:n.4739A>T
ENST00000566605.5:c.*737A>T	ENSP00000455073.1:n.*737A>T
ENST00000568685.1:c.1567A>T	ENSP00000455282.1:p.Arg523Trp
ENST00000569760.5:n.455A>T
NM_001170634.1:c.1561A>T	NP_001164105.1:p.Arg521Trp
NM_001170937.1:c.1552A>T	NP_001164408.1:p.Arg518Trp
NM_004960.3:c.1564A>T , LRG_655t1:c.1564A>T	NP_004951.1:p.Arg522Trp
NR_028388.2:n.1634A>T
XM_005255233.3:c.949A>T	XP_005255290.1:p.Arg317Trp
XM_011545781.1:c.1558A>T	XP_011544083.1:p.Arg520Trp
XM_011545782.1:c.949A>T	XP_011544084.1:p.Arg317Trp
XM_005255233.5:c.949A>T	XP_005255290.1:p.Arg317Trp
XM_011545782.2:c.949A>T	XP_011544084.1:p.Arg317Trp
XM_024450221.1:c.1555A>T	XP_024305989.1:p.Arg519Trp
NM_004960.4:c.1564A>T MANE Select	NP_004951.1:p.Arg522Trp