Canonical Allele Identifier: CA395677437

Gene: FUS

Linked Data

• dbSNP Id: rs121909668
• MyVariant Identifiers: chr16:g.31202739C>A (hg19) ; chr16:g.31191418C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31191418C>A , CM000678.2:g.31191418C>A	GRCh38
NC_000016.9:g.31202739C>A , CM000678.1:g.31202739C>A	GRCh37
NC_000016.8:g.31110240C>A	NCBI36
NG_012889.2:g.16287C>A , LRG_655:g.16287C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000254108.12:c.1561C>A MANE Select	ENSP00000254108.8:p.Arg521Ser
ENST00000254108.11:c.1561C>A	ENSP00000254108.7:p.Arg521Ser
ENST00000380244.7:c.1558C>A	ENSP00000369594.3:p.Arg520Ser
ENST00000483853.1:n.638C>A
ENST00000487509.6:n.4736C>A
ENST00000566605.5:c.*734C>A	ENSP00000455073.1:n.*734C>A
ENST00000568685.1:c.1564C>A	ENSP00000455282.1:p.Arg522Ser
ENST00000569760.5:n.452C>A
NM_001170634.1:c.1558C>A	NP_001164105.1:p.Arg520Ser
NM_001170937.1:c.1549C>A	NP_001164408.1:p.Arg517Ser
NM_004960.3:c.1561C>A , LRG_655t1:c.1561C>A	NP_004951.1:p.Arg521Ser
NR_028388.2:n.1631C>A
XM_005255233.3:c.946C>A	XP_005255290.1:p.Arg316Ser
XM_011545781.1:c.1555C>A	XP_011544083.1:p.Arg519Ser
XM_011545782.1:c.946C>A	XP_011544084.1:p.Arg316Ser
XM_005255233.5:c.946C>A	XP_005255290.1:p.Arg316Ser
XM_011545782.2:c.946C>A	XP_011544084.1:p.Arg316Ser
XM_024450221.1:c.1552C>A	XP_024305989.1:p.Arg518Ser
NM_004960.4:c.1561C>A MANE Select	NP_004951.1:p.Arg521Ser