Canonical Allele Identifier: CA2216947197

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189249_31189253delinsGCTTT , CM000678.2:g.31189249_31189253delinsGCTTT	GRCh38
NC_000016.9:g.31200570_31200574delinsGCTTT , CM000678.1:g.31200570_31200574delinsGCTTT	GRCh37
NC_000016.8:g.31108071_31108075delinsGCTTT	NCBI36
NG_012889.2:g.14118_14122delinsGCTTT , LRG_655:g.14118_14122delinsGCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.936+23_936+27delinsGCTTT MANE Select	ENSP00000254108.8:n.936+23_936+27delinsGCTTT
ENST00000254108.11:c.936+23_936+27delinsGCTTT	ENSP00000254108.7:n.936+23_936+27delinsGCTTT
ENST00000380244.7:c.933+23_933+27delinsGCTTT	ENSP00000369594.3:n.933+23_933+27delinsGCTTT
ENST00000474990.5:n.230+23_230+27delinsGCTTT
ENST00000487509.6:n.4111+23_4111+27delinsGCTTT
ENST00000564766.1:n.760+23_760+27delinsGCTTT
ENST00000566605.5:c.*109+23_*109+27delinsGCTTT	ENSP00000455073.1:n.*109+23_*109+27delinsGCTTT
ENST00000568685.1:c.939+23_939+27delinsGCTTT	ENSP00000455282.1:n.939+23_939+27delinsGCTTT
ENST00000568901.2:n.310+23_310+27delinsGCTTT
NM_001170634.1:c.933+23_933+27delinsGCTTT	NP_001164105.1:n.933+23_933+27delinsGCTTT
NM_001170937.1:c.924+23_924+27delinsGCTTT	NP_001164408.1:n.924+23_924+27delinsGCTTT
NM_004960.3:c.936+23_936+27delinsGCTTT , LRG_655t1:c.936+23_936+27delinsGCTTT	NP_004951.1:n.936+23_936+27delinsGCTTT
NR_028388.2:n.1006+23_1006+27delinsGCTTT
XM_005255233.3:c.321+23_321+27delinsGCTTT	XP_005255290.1:n.321+23_321+27delinsGCTTT
XM_011545781.1:c.930+23_930+27delinsGCTTT	XP_011544083.1:n.930+23_930+27delinsGCTTT
XM_011545782.1:c.321+23_321+27delinsGCTTT	XP_011544084.1:n.321+23_321+27delinsGCTTT
XM_005255233.5:c.321+23_321+27delinsGCTTT	XP_005255290.1:n.321+23_321+27delinsGCTTT
XM_011545782.2:c.321+23_321+27delinsGCTTT	XP_011544084.1:n.321+23_321+27delinsGCTTT
XM_024450221.1:c.927+23_927+27delinsGCTTT	XP_024305989.1:n.927+23_927+27delinsGCTTT
NM_004960.4:c.936+23_936+27delinsGCTTT MANE Select	NP_004951.1:n.936+23_936+27delinsGCTTT