Canonical Allele Identifier: CA8023857

Gene: FUS

Linked Data

• ClinVar Variation Id: 1204463
• ClinVar RCV Id: RCV001570817
• dbSNP Id: rs77308300
• ExAC: 16:31200401 A / G
• gnomAD v2: 16-31200401-A-G
• gnomAD v3: 16-31189080-A-G
• gnomAD v4: 16-31189080-A-G
• MyVariant Identifiers: chr16:g.31200401A>G (hg19) ; chr16:g.31189080A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189080A>G , CM000678.2:g.31189080A>G	GRCh38
NC_000016.9:g.31200401A>G , CM000678.1:g.31200401A>G	GRCh37
NC_000016.8:g.31107902A>G	NCBI36
NG_012889.2:g.13949A>G , LRG_655:g.13949A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.833-43A>G MANE Select	ENSP00000254108.8:n.833-43A>G
ENST00000254108.11:c.833-43A>G	ENSP00000254108.7:n.833-43A>G
ENST00000380244.7:c.830-43A>G	ENSP00000369594.3:n.830-43A>G
ENST00000474990.5:n.127-43A>G
ENST00000487509.6:n.4008-43A>G
ENST00000564766.1:n.614A>G
ENST00000566605.5:c.*6-43A>G	ENSP00000455073.1:n.*6-43A>G
ENST00000568685.1:c.833-40A>G	ENSP00000455282.1:n.833-40A>G
ENST00000568901.2:n.207-43A>G
NM_001170634.1:c.830-43A>G	NP_001164105.1:n.830-43A>G
NM_001170937.1:c.821-43A>G	NP_001164408.1:n.821-43A>G
NM_004960.3:c.833-43A>G , LRG_655t1:c.833-43A>G	NP_004951.1:n.833-43A>G
NR_028388.2:n.903-43A>G
XM_005255233.3:c.218-43A>G	XP_005255290.1:n.218-43A>G
XM_011545781.1:c.827-43A>G	XP_011544083.1:n.827-43A>G
XM_011545782.1:c.218-43A>G	XP_011544084.1:n.218-43A>G
XM_005255233.5:c.218-43A>G	XP_005255290.1:n.218-43A>G
XM_011545782.2:c.218-43A>G	XP_011544084.1:n.218-43A>G
XM_024450221.1:c.824-43A>G	XP_024305989.1:n.824-43A>G
NM_004960.4:c.833-43A>G MANE Select	NP_004951.1:n.833-43A>G