Canonical Allele Identifier: CA2632839996
Gene: FUS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31189356_31189357del , CM000678.2:g.31189356_31189357del GRCh38
NC_000016.9:g.31200677_31200678del , CM000678.1:g.31200677_31200678del GRCh37
NC_000016.8:g.31108178_31108179del NCBI36
NG_012889.2:g.14225_14226del , LRG_655:g.14225_14226del

Transcript Alleles

HGVS Amino-acid Change
ENST00000254108.12:c.936+130_936+131del MANE Select ENSP00000254108.8:n.936+130_936+131del
ENST00000254108.11:c.936+130_936+131del ENSP00000254108.7:n.936+130_936+131del
ENST00000380244.7:c.933+130_933+131del ENSP00000369594.3:n.933+130_933+131del
ENST00000474990.5:n.230+130_230+131del
ENST00000487509.6:n.4111+130_4111+131del
ENST00000564766.1:n.760+130_760+131del
ENST00000566605.5:c.*109+130_*109+131del ENSP00000455073.1:n.*109+130_*109+131del
ENST00000568685.1:c.939+130_939+131del ENSP00000455282.1:n.939+130_939+131del
ENST00000568901.2:n.310+130_310+131del
NM_001170634.1:c.933+130_933+131del NP_001164105.1:n.933+130_933+131del
NM_001170937.1:c.924+130_924+131del NP_001164408.1:n.924+130_924+131del
NM_004960.3:c.936+130_936+131del , LRG_655t1:c.936+130_936+131del NP_004951.1:n.936+130_936+131del
NR_028388.2:n.1006+130_1006+131del
XM_005255233.3:c.321+130_321+131del XP_005255290.1:n.321+130_321+131del
XM_011545781.1:c.930+130_930+131del XP_011544083.1:n.930+130_930+131del
XM_011545782.1:c.321+130_321+131del XP_011544084.1:n.321+130_321+131del
XM_005255233.5:c.321+130_321+131del XP_005255290.1:n.321+130_321+131del
XM_011545782.2:c.321+130_321+131del XP_011544084.1:n.321+130_321+131del
XM_024450221.1:c.927+130_927+131del XP_024305989.1:n.927+130_927+131del
NM_004960.4:c.936+130_936+131del MANE Select NP_004951.1:n.936+130_936+131del