Canonical Allele Identifier: CA8023697

Gene: FUS

Linked Data

• ClinVar Variation Id: 2940324
• ClinVar RCV Id: RCV003797682
• dbSNP Id: rs755045476
• ExAC: 16:31196244 CT / C
• gnomAD v2: 16-31196244-CT-C
• gnomAD v3: 16-31184923-CT-C
• gnomAD v4: 16-31184923-CT-C
• MyVariant Identifiers: chr16:g.31196245del (hg19) ; chr16:g.31184924del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31184926del , CM000678.2:g.31184926del	GRCh38
NC_000016.9:g.31196247del , CM000678.1:g.31196247del	GRCh37
NC_000016.8:g.31103748del	NCBI36
NG_012889.2:g.9795del , LRG_655:g.9795del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.524-13del MANE Select	ENSP00000254108.8:n.524-13del
ENST00000254108.11:c.524-13del	ENSP00000254108.7:n.524-13del
ENST00000380244.7:c.521-13del	ENSP00000369594.3:n.521-13del
ENST00000487509.6:n.589-13del
ENST00000566605.5:c.524-13del	ENSP00000455073.1:n.524-13del
ENST00000568685.1:c.524-13del	ENSP00000455282.1:n.524-13del
NM_001170634.1:c.521-13del	NP_001164105.1:n.521-13del
NM_001170937.1:c.512-13del	NP_001164408.1:n.512-13del
NM_004960.3:c.524-13del , LRG_655t1:c.524-13del	NP_004951.1:n.524-13del
NR_028388.2:n.629-13del
XM_005255233.3:c.-57-13del	XP_005255290.1:n.-57-13del
XM_011545781.1:c.518-13del	XP_011544083.1:n.518-13del
XM_011545782.1:c.-57-13del	XP_011544084.1:n.-57-13del
XM_005255233.5:c.-57-13del	XP_005255290.1:n.-57-13del
XM_011545782.2:c.-57-13del	XP_011544084.1:n.-57-13del
XM_024450221.1:c.515-13del	XP_024305989.1:n.515-13del
NM_004960.4:c.524-13del MANE Select	NP_004951.1:n.524-13del