Canonical Allele Identifier: CA395672235

Gene: FUS

Linked Data

• ClinVar Variation Id: 2922331
• ClinVar RCV Id: RCV003785545
• gnomAD v4: 16-31189174-A-G
• MyVariant Identifiers: chr16:g.31200495A>G (hg19) ; chr16:g.31189174A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189174A>G , CM000678.2:g.31189174A>G	GRCh38
NC_000016.9:g.31200495A>G , CM000678.1:g.31200495A>G	GRCh37
NC_000016.8:g.31107996A>G	NCBI36
NG_012889.2:g.14043A>G , LRG_655:g.14043A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.884A>G MANE Select	ENSP00000254108.8:p.Asn295Ser
ENST00000254108.11:c.884A>G	ENSP00000254108.7:p.Asn295Ser
ENST00000380244.7:c.881A>G	ENSP00000369594.3:p.Asn294Ser
ENST00000474990.5:n.178A>G
ENST00000487509.6:n.4059A>G
ENST00000564766.1:n.708A>G
ENST00000566605.5:c.*57A>G	ENSP00000455073.1:n.*57A>G
ENST00000568685.1:c.887A>G	ENSP00000455282.1:p.Asn296Ser
ENST00000568901.2:n.258A>G
NM_001170634.1:c.881A>G	NP_001164105.1:p.Asn294Ser
NM_001170937.1:c.872A>G	NP_001164408.1:p.Asn291Ser
NM_004960.3:c.884A>G , LRG_655t1:c.884A>G	NP_004951.1:p.Asn295Ser
NR_028388.2:n.954A>G
XM_005255233.3:c.269A>G	XP_005255290.1:p.Asn90Ser
XM_011545781.1:c.878A>G	XP_011544083.1:p.Asn293Ser
XM_011545782.1:c.269A>G	XP_011544084.1:p.Asn90Ser
XM_005255233.5:c.269A>G	XP_005255290.1:p.Asn90Ser
XM_011545782.2:c.269A>G	XP_011544084.1:p.Asn90Ser
XM_024450221.1:c.875A>G	XP_024305989.1:p.Asn292Ser
NM_004960.4:c.884A>G MANE Select	NP_004951.1:p.Asn295Ser