Canonical Allele Identifier: CA2528454950

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189364dup , CM000678.2:g.31189364dup	GRCh38
NC_000016.9:g.31200685dup , CM000678.1:g.31200685dup	GRCh37
NC_000016.8:g.31108186dup	NCBI36
NG_012889.2:g.14233dup , LRG_655:g.14233dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.936+138dup MANE Select	ENSP00000254108.8:n.936+138dup
ENST00000254108.11:c.936+138dup	ENSP00000254108.7:n.936+138dup
ENST00000380244.7:c.933+138dup	ENSP00000369594.3:n.933+138dup
ENST00000474990.5:n.230+138dup
ENST00000487509.6:n.4111+138dup
ENST00000564766.1:n.760+138dup
ENST00000566605.5:c.*109+138dup	ENSP00000455073.1:n.*109+138dup
ENST00000568685.1:c.939+138dup	ENSP00000455282.1:n.939+138dup
ENST00000568901.2:n.310+138dup
NM_001170634.1:c.933+138dup	NP_001164105.1:n.933+138dup
NM_001170937.1:c.924+138dup	NP_001164408.1:n.924+138dup
NM_004960.3:c.936+138dup , LRG_655t1:c.936+138dup	NP_004951.1:n.936+138dup
NR_028388.2:n.1006+138dup
XM_005255233.3:c.321+138dup	XP_005255290.1:n.321+138dup
XM_011545781.1:c.930+138dup	XP_011544083.1:n.930+138dup
XM_011545782.1:c.321+138dup	XP_011544084.1:n.321+138dup
XM_005255233.5:c.321+138dup	XP_005255290.1:n.321+138dup
XM_011545782.2:c.321+138dup	XP_011544084.1:n.321+138dup
XM_024450221.1:c.927+138dup	XP_024305989.1:n.927+138dup
NM_004960.4:c.936+138dup MANE Select	NP_004951.1:n.936+138dup