Canonical Allele Identifier: CA395672381

Gene: FUS

Linked Data

• dbSNP Id: rs1380069668
• gnomAD v3: 16-31189197-G-A
• gnomAD v4: 16-31189197-G-A
• MyVariant Identifiers: chr16:g.31200518G>A (hg19) ; chr16:g.31189197G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189197G>A , CM000678.2:g.31189197G>A	GRCh38
NC_000016.9:g.31200518G>A , CM000678.1:g.31200518G>A	GRCh37
NC_000016.8:g.31108019G>A	NCBI36
NG_012889.2:g.14066G>A , LRG_655:g.14066G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.907G>A MANE Select	ENSP00000254108.8:p.Asp303Asn
ENST00000254108.11:c.907G>A	ENSP00000254108.7:p.Asp303Asn
ENST00000380244.7:c.904G>A	ENSP00000369594.3:p.Asp302Asn
ENST00000474990.5:n.201G>A
ENST00000487509.6:n.4082G>A
ENST00000564766.1:n.731G>A
ENST00000566605.5:c.*80G>A	ENSP00000455073.1:n.*80G>A
ENST00000568685.1:c.910G>A	ENSP00000455282.1:p.Asp304Asn
ENST00000568901.2:n.281G>A
NM_001170634.1:c.904G>A	NP_001164105.1:p.Asp302Asn
NM_001170937.1:c.895G>A	NP_001164408.1:p.Asp299Asn
NM_004960.3:c.907G>A , LRG_655t1:c.907G>A	NP_004951.1:p.Asp303Asn
NR_028388.2:n.977G>A
XM_005255233.3:c.292G>A	XP_005255290.1:p.Asp98Asn
XM_011545781.1:c.901G>A	XP_011544083.1:p.Asp301Asn
XM_011545782.1:c.292G>A	XP_011544084.1:p.Asp98Asn
XM_005255233.5:c.292G>A	XP_005255290.1:p.Asp98Asn
XM_011545782.2:c.292G>A	XP_011544084.1:p.Asp98Asn
XM_024450221.1:c.898G>A	XP_024305989.1:p.Asp300Asn
NM_004960.4:c.907G>A MANE Select	NP_004951.1:p.Asp303Asn