Canonical Allele Identifier: CA2216947265
Gene: FUS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31189379_31189381delinsACT , CM000678.2:g.31189379_31189381delinsACT GRCh38
NC_000016.9:g.31200700_31200702delinsACT , CM000678.1:g.31200700_31200702delinsACT GRCh37
NC_000016.8:g.31108201_31108203delinsACT NCBI36
NG_012889.2:g.14248_14250delinsACT , LRG_655:g.14248_14250delinsACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000254108.12:c.936+153_936+155delinsACT MANE Select ENSP00000254108.8:n.936+153_936+155delinsACT
ENST00000254108.11:c.936+153_936+155delinsACT ENSP00000254108.7:n.936+153_936+155delinsACT
ENST00000380244.7:c.933+153_933+155delinsACT ENSP00000369594.3:n.933+153_933+155delinsACT
ENST00000474990.5:n.230+153_230+155delinsACT
ENST00000487509.6:n.4111+153_4111+155delinsACT
ENST00000564766.1:n.760+153_760+155delinsACT
ENST00000566605.5:c.*109+153_*109+155delinsACT ENSP00000455073.1:n.*109+153_*109+155delinsACT
ENST00000568685.1:c.939+153_939+155delinsACT ENSP00000455282.1:n.939+153_939+155delinsACT
ENST00000568901.2:n.310+153_310+155delinsACT
NM_001170634.1:c.933+153_933+155delinsACT NP_001164105.1:n.933+153_933+155delinsACT
NM_001170937.1:c.924+153_924+155delinsACT NP_001164408.1:n.924+153_924+155delinsACT
NM_004960.3:c.936+153_936+155delinsACT , LRG_655t1:c.936+153_936+155delinsACT NP_004951.1:n.936+153_936+155delinsACT
NR_028388.2:n.1006+153_1006+155delinsACT
XM_005255233.3:c.321+153_321+155delinsACT XP_005255290.1:n.321+153_321+155delinsACT
XM_011545781.1:c.930+153_930+155delinsACT XP_011544083.1:n.930+153_930+155delinsACT
XM_011545782.1:c.321+153_321+155delinsACT XP_011544084.1:n.321+153_321+155delinsACT
XM_005255233.5:c.321+153_321+155delinsACT XP_005255290.1:n.321+153_321+155delinsACT
XM_011545782.2:c.321+153_321+155delinsACT XP_011544084.1:n.321+153_321+155delinsACT
XM_024450221.1:c.927+153_927+155delinsACT XP_024305989.1:n.927+153_927+155delinsACT
NM_004960.4:c.936+153_936+155delinsACT MANE Select NP_004951.1:n.936+153_936+155delinsACT