Canonical Allele Identifier: CA395677387

Gene: FUS

Linked Data

• ClinVar Variation Id: 650787
• ClinVar RCV Id: RCV000806009
• dbSNP Id: rs1567479067
• MyVariant Identifiers: chr16:g.31202733C>G (hg19) ; chr16:g.31191412C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31191412C>G , CM000678.2:g.31191412C>G	GRCh38
NC_000016.9:g.31202733C>G , CM000678.1:g.31202733C>G	GRCh37
NC_000016.8:g.31110234C>G	NCBI36
NG_012889.2:g.16281C>G , LRG_655:g.16281C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000254108.12:c.1555C>G MANE Select	ENSP00000254108.8:p.Gln519Glu
ENST00000254108.11:c.1555C>G	ENSP00000254108.7:p.Gln519Glu
ENST00000380244.7:c.1552C>G	ENSP00000369594.3:p.Gln518Glu
ENST00000483853.1:n.632C>G
ENST00000487509.6:n.4730C>G
ENST00000566605.5:c.*728C>G	ENSP00000455073.1:n.*728C>G
ENST00000568685.1:c.1558C>G	ENSP00000455282.1:p.Gln520Glu
ENST00000569760.5:n.446C>G
NM_001170634.1:c.1552C>G	NP_001164105.1:p.Gln518Glu
NM_001170937.1:c.1543C>G	NP_001164408.1:p.Gln515Glu
NM_004960.3:c.1555C>G , LRG_655t1:c.1555C>G	NP_004951.1:p.Gln519Glu
NR_028388.2:n.1625C>G
XM_005255233.3:c.940C>G	XP_005255290.1:p.Gln314Glu
XM_011545781.1:c.1549C>G	XP_011544083.1:p.Gln517Glu
XM_011545782.1:c.940C>G	XP_011544084.1:p.Gln314Glu
XM_005255233.5:c.940C>G	XP_005255290.1:p.Gln314Glu
XM_011545782.2:c.940C>G	XP_011544084.1:p.Gln314Glu
XM_024450221.1:c.1546C>G	XP_024305989.1:p.Gln516Glu
NM_004960.4:c.1555C>G MANE Select	NP_004951.1:p.Gln519Glu