Canonical Allele Identifier: CA10603525

Gene: FUS

Linked Data

• ClinVar Variation Id: 280356
• ClinVar RCV Id: RCV000395608
• dbSNP Id: rs886041577
• MyVariant Identifiers: chr16:g.31202394_31202395del (hg19) ; chr16:g.31191073_31191074del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31191073_31191074del , CM000678.2:g.31191073_31191074del	GRCh38
NC_000016.9:g.31202394_31202395del , CM000678.1:g.31202394_31202395del	GRCh37
NC_000016.8:g.31109895_31109896del	NCBI36
NG_012889.2:g.15942_15943del , LRG_655:g.15942_15943del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.1504_1505del MANE Select	ENSP00000254108.8:p.Asp502GlnfsTer14
ENST00000254108.11:c.1504_1505del	ENSP00000254108.7:p.Asp502GlnfsTer14
ENST00000380244.7:c.1501_1502del	ENSP00000369594.3:p.Asp501GlnfsTer14
ENST00000474990.5:n.798_799del
ENST00000483853.1:n.581_582del
ENST00000487509.6:n.4679_4680del
ENST00000566605.5:c.*677_*678del	ENSP00000455073.1:n.*677_*678del
ENST00000568685.1:c.1507_1508del	ENSP00000455282.1:p.Asp503GlnfsTer14
ENST00000569760.5:n.395_396del
NM_001170634.1:c.1501_1502del	NP_001164105.1:p.Asp501GlnfsTer14
NM_001170937.1:c.1492_1493del	NP_001164408.1:p.Asp498GlnfsTer14
NM_004960.3:c.1504_1505del , LRG_655t1:c.1504_1505del	NP_004951.1:p.Asp502GlnfsTer14
NR_028388.2:n.1574_1575del
XM_005255233.3:c.889_890del	XP_005255290.1:p.Asp297GlnfsTer14
XM_011545781.1:c.1498_1499del	XP_011544083.1:p.Asp500GlnfsTer14
XM_011545782.1:c.889_890del	XP_011544084.1:p.Asp297GlnfsTer14
XM_005255233.5:c.889_890del	XP_005255290.1:p.Asp297GlnfsTer14
XM_011545782.2:c.889_890del	XP_011544084.1:p.Asp297GlnfsTer14
XM_024450221.1:c.1495_1496del	XP_024305989.1:p.Asp499GlnfsTer14
NM_004960.4:c.1504_1505del MANE Select	NP_004951.1:p.Asp502GlnfsTer14