Canonical Allele Identifier: CA395669495

Gene: FUS

Linked Data

• dbSNP Id: rs1177254702
• gnomAD v2: 16-31196264-C-G
• gnomAD v4: 16-31184943-C-G
• MyVariant Identifiers: chr16:g.31196264C>G (hg19) ; chr16:g.31184943C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31184943C>G , CM000678.2:g.31184943C>G	GRCh38
NC_000016.9:g.31196264C>G , CM000678.1:g.31196264C>G	GRCh37
NC_000016.8:g.31103765C>G	NCBI36
NG_012889.2:g.9812C>G , LRG_655:g.9812C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.528C>G MANE Select	ENSP00000254108.8:p.Asn176Lys
ENST00000254108.11:c.528C>G	ENSP00000254108.7:p.Asn176Lys
ENST00000380244.7:c.525C>G	ENSP00000369594.3:p.Asn175Lys
ENST00000487509.6:n.593C>G
ENST00000566605.5:c.528C>G	ENSP00000455073.1:p.Asn176Lys
ENST00000568685.1:c.528C>G	ENSP00000455282.1:p.Asn176Lys
NM_001170634.1:c.525C>G	NP_001164105.1:p.Asn175Lys
NM_001170937.1:c.516C>G	NP_001164408.1:p.Asn172Lys
NM_004960.3:c.528C>G , LRG_655t1:c.528C>G	NP_004951.1:p.Asn176Lys
NR_028388.2:n.633C>G
XM_005255233.3:c.-53C>G	XP_005255290.1:n.-53C>G
XM_011545781.1:c.522C>G	XP_011544083.1:p.Asn174Lys
XM_011545782.1:c.-53C>G	XP_011544084.1:n.-53C>G
XM_005255233.5:c.-53C>G	XP_005255290.1:n.-53C>G
XM_011545782.2:c.-53C>G	XP_011544084.1:n.-53C>G
XM_024450221.1:c.519C>G	XP_024305989.1:p.Asn173Lys
NM_004960.4:c.528C>G MANE Select	NP_004951.1:p.Asn176Lys