Canonical Allele Identifier: CA395669475

Gene: FUS

Linked Data

• gnomAD v4: 16-31184941-A-G
• MyVariant Identifiers: chr16:g.31196262A>G (hg19) ; chr16:g.31184941A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31184941A>G , CM000678.2:g.31184941A>G	GRCh38
NC_000016.9:g.31196262A>G , CM000678.1:g.31196262A>G	GRCh37
NC_000016.8:g.31103763A>G	NCBI36
NG_012889.2:g.9810A>G , LRG_655:g.9810A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.526A>G MANE Select	ENSP00000254108.8:p.Asn176Asp
ENST00000254108.11:c.526A>G	ENSP00000254108.7:p.Asn176Asp
ENST00000380244.7:c.523A>G	ENSP00000369594.3:p.Asn175Asp
ENST00000487509.6:n.591A>G
ENST00000566605.5:c.526A>G	ENSP00000455073.1:p.Asn176Asp
ENST00000568685.1:c.526A>G	ENSP00000455282.1:p.Asn176Asp
NM_001170634.1:c.523A>G	NP_001164105.1:p.Asn175Asp
NM_001170937.1:c.514A>G	NP_001164408.1:p.Asn172Asp
NM_004960.3:c.526A>G , LRG_655t1:c.526A>G	NP_004951.1:p.Asn176Asp
NR_028388.2:n.631A>G
XM_005255233.3:c.-55A>G	XP_005255290.1:n.-55A>G
XM_011545781.1:c.520A>G	XP_011544083.1:p.Asn174Asp
XM_011545782.1:c.-55A>G	XP_011544084.1:n.-55A>G
XM_005255233.5:c.-55A>G	XP_005255290.1:n.-55A>G
XM_011545782.2:c.-55A>G	XP_011544084.1:n.-55A>G
XM_024450221.1:c.517A>G	XP_024305989.1:p.Asn173Asp
NM_004960.4:c.526A>G MANE Select	NP_004951.1:p.Asn176Asp