Canonical Allele Identifier: CA2216944322

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31184923_31184924delinsCT , CM000678.2:g.31184923_31184924delinsCT	GRCh38
NC_000016.9:g.31196244_31196245delinsCT , CM000678.1:g.31196244_31196245delinsCT	GRCh37
NC_000016.8:g.31103745_31103746delinsCT	NCBI36
NG_012889.2:g.9792_9793delinsCT , LRG_655:g.9792_9793delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.524-16_524-15delinsCT MANE Select	ENSP00000254108.8:n.524-16_524-15delinsCT
ENST00000254108.11:c.524-16_524-15delinsCT	ENSP00000254108.7:n.524-16_524-15delinsCT
ENST00000380244.7:c.521-16_521-15delinsCT	ENSP00000369594.3:n.521-16_521-15delinsCT
ENST00000487509.6:n.589-16_589-15delinsCT
ENST00000566605.5:c.524-16_524-15delinsCT	ENSP00000455073.1:n.524-16_524-15delinsCT
ENST00000568685.1:c.524-16_524-15delinsCT	ENSP00000455282.1:n.524-16_524-15delinsCT
NM_001170634.1:c.521-16_521-15delinsCT	NP_001164105.1:n.521-16_521-15delinsCT
NM_001170937.1:c.512-16_512-15delinsCT	NP_001164408.1:n.512-16_512-15delinsCT
NM_004960.3:c.524-16_524-15delinsCT , LRG_655t1:c.524-16_524-15delinsCT	NP_004951.1:n.524-16_524-15delinsCT
NR_028388.2:n.629-16_629-15delinsCT
XM_005255233.3:c.-57-16_-57-15delinsCT	XP_005255290.1:n.-57-16_-57-15delinsCT
XM_011545781.1:c.518-16_518-15delinsCT	XP_011544083.1:n.518-16_518-15delinsCT
XM_011545782.1:c.-57-16_-57-15delinsCT	XP_011544084.1:n.-57-16_-57-15delinsCT
XM_005255233.5:c.-57-16_-57-15delinsCT	XP_005255290.1:n.-57-16_-57-15delinsCT
XM_011545782.2:c.-57-16_-57-15delinsCT	XP_011544084.1:n.-57-16_-57-15delinsCT
XM_024450221.1:c.515-16_515-15delinsCT	XP_024305989.1:n.515-16_515-15delinsCT
NM_004960.4:c.524-16_524-15delinsCT MANE Select	NP_004951.1:n.524-16_524-15delinsCT