Canonical Allele Identifier: CA2216947185

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189230_31189231delinsCT , CM000678.2:g.31189230_31189231delinsCT	GRCh38
NC_000016.9:g.31200551_31200552delinsCT , CM000678.1:g.31200551_31200552delinsCT	GRCh37
NC_000016.8:g.31108052_31108053delinsCT	NCBI36
NG_012889.2:g.14099_14100delinsCT , LRG_655:g.14099_14100delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.936+4_936+5delinsCT MANE Select	ENSP00000254108.8:n.936+4_936+5delinsCT
ENST00000254108.11:c.936+4_936+5delinsCT	ENSP00000254108.7:n.936+4_936+5delinsCT
ENST00000380244.7:c.933+4_933+5delinsCT	ENSP00000369594.3:n.933+4_933+5delinsCT
ENST00000474990.5:n.230+4_230+5delinsCT
ENST00000487509.6:n.4111+4_4111+5delinsCT
ENST00000564766.1:n.760+4_760+5delinsCT
ENST00000566605.5:c.*109+4_*109+5delinsCT	ENSP00000455073.1:n.*109+4_*109+5delinsCT
ENST00000568685.1:c.939+4_939+5delinsCT	ENSP00000455282.1:n.939+4_939+5delinsCT
ENST00000568901.2:n.310+4_310+5delinsCT
NM_001170634.1:c.933+4_933+5delinsCT	NP_001164105.1:n.933+4_933+5delinsCT
NM_001170937.1:c.924+4_924+5delinsCT	NP_001164408.1:n.924+4_924+5delinsCT
NM_004960.3:c.936+4_936+5delinsCT , LRG_655t1:c.936+4_936+5delinsCT	NP_004951.1:n.936+4_936+5delinsCT
NR_028388.2:n.1006+4_1006+5delinsCT
XM_005255233.3:c.321+4_321+5delinsCT	XP_005255290.1:n.321+4_321+5delinsCT
XM_011545781.1:c.930+4_930+5delinsCT	XP_011544083.1:n.930+4_930+5delinsCT
XM_011545782.1:c.321+4_321+5delinsCT	XP_011544084.1:n.321+4_321+5delinsCT
XM_005255233.5:c.321+4_321+5delinsCT	XP_005255290.1:n.321+4_321+5delinsCT
XM_011545782.2:c.321+4_321+5delinsCT	XP_011544084.1:n.321+4_321+5delinsCT
XM_024450221.1:c.927+4_927+5delinsCT	XP_024305989.1:n.927+4_927+5delinsCT
NM_004960.4:c.936+4_936+5delinsCT MANE Select	NP_004951.1:n.936+4_936+5delinsCT