Canonical Allele Identifier: CA2216944220

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31184866_31184867delinsCT , CM000678.2:g.31184866_31184867delinsCT	GRCh38
NC_000016.9:g.31196187_31196188delinsCT , CM000678.1:g.31196187_31196188delinsCT	GRCh37
NC_000016.8:g.31103688_31103689delinsCT	NCBI36
NG_012889.2:g.9735_9736delinsCT , LRG_655:g.9735_9736delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.524-73_524-72delinsCT MANE Select	ENSP00000254108.8:n.524-73_524-72delinsCT
ENST00000254108.11:c.524-73_524-72delinsCT	ENSP00000254108.7:n.524-73_524-72delinsCT
ENST00000380244.7:c.521-73_521-72delinsCT	ENSP00000369594.3:n.521-73_521-72delinsCT
ENST00000487509.6:n.589-73_589-72delinsCT
ENST00000566605.5:c.524-73_524-72delinsCT	ENSP00000455073.1:n.524-73_524-72delinsCT
ENST00000568685.1:c.524-73_524-72delinsCT	ENSP00000455282.1:n.524-73_524-72delinsCT
NM_001170634.1:c.521-73_521-72delinsCT	NP_001164105.1:n.521-73_521-72delinsCT
NM_001170937.1:c.512-73_512-72delinsCT	NP_001164408.1:n.512-73_512-72delinsCT
NM_004960.3:c.524-73_524-72delinsCT , LRG_655t1:c.524-73_524-72delinsCT	NP_004951.1:n.524-73_524-72delinsCT
NR_028388.2:n.629-73_629-72delinsCT
XM_005255233.3:c.-57-73_-57-72delinsCT	XP_005255290.1:n.-57-73_-57-72delinsCT
XM_011545781.1:c.518-73_518-72delinsCT	XP_011544083.1:n.518-73_518-72delinsCT
XM_011545782.1:c.-57-73_-57-72delinsCT	XP_011544084.1:n.-57-73_-57-72delinsCT
XM_005255233.5:c.-57-73_-57-72delinsCT	XP_005255290.1:n.-57-73_-57-72delinsCT
XM_011545782.2:c.-57-73_-57-72delinsCT	XP_011544084.1:n.-57-73_-57-72delinsCT
XM_024450221.1:c.515-73_515-72delinsCT	XP_024305989.1:n.515-73_515-72delinsCT
NM_004960.4:c.524-73_524-72delinsCT MANE Select	NP_004951.1:n.524-73_524-72delinsCT