Canonical Allele Identifier: CA2216947262
Gene: FUS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31189374_31189375delinsTA , CM000678.2:g.31189374_31189375delinsTA GRCh38
NC_000016.9:g.31200695_31200696delinsTA , CM000678.1:g.31200695_31200696delinsTA GRCh37
NC_000016.8:g.31108196_31108197delinsTA NCBI36
NG_012889.2:g.14243_14244delinsTA , LRG_655:g.14243_14244delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000254108.12:c.936+148_936+149delinsTA MANE Select ENSP00000254108.8:n.936+148_936+149delinsTA
ENST00000254108.11:c.936+148_936+149delinsTA ENSP00000254108.7:n.936+148_936+149delinsTA
ENST00000380244.7:c.933+148_933+149delinsTA ENSP00000369594.3:n.933+148_933+149delinsTA
ENST00000474990.5:n.230+148_230+149delinsTA
ENST00000487509.6:n.4111+148_4111+149delinsTA
ENST00000564766.1:n.760+148_760+149delinsTA
ENST00000566605.5:c.*109+148_*109+149delinsTA ENSP00000455073.1:n.*109+148_*109+149delinsTA
ENST00000568685.1:c.939+148_939+149delinsTA ENSP00000455282.1:n.939+148_939+149delinsTA
ENST00000568901.2:n.310+148_310+149delinsTA
NM_001170634.1:c.933+148_933+149delinsTA NP_001164105.1:n.933+148_933+149delinsTA
NM_001170937.1:c.924+148_924+149delinsTA NP_001164408.1:n.924+148_924+149delinsTA
NM_004960.3:c.936+148_936+149delinsTA , LRG_655t1:c.936+148_936+149delinsTA NP_004951.1:n.936+148_936+149delinsTA
NR_028388.2:n.1006+148_1006+149delinsTA
XM_005255233.3:c.321+148_321+149delinsTA XP_005255290.1:n.321+148_321+149delinsTA
XM_011545781.1:c.930+148_930+149delinsTA XP_011544083.1:n.930+148_930+149delinsTA
XM_011545782.1:c.321+148_321+149delinsTA XP_011544084.1:n.321+148_321+149delinsTA
XM_005255233.5:c.321+148_321+149delinsTA XP_005255290.1:n.321+148_321+149delinsTA
XM_011545782.2:c.321+148_321+149delinsTA XP_011544084.1:n.321+148_321+149delinsTA
XM_024450221.1:c.927+148_927+149delinsTA XP_024305989.1:n.927+148_927+149delinsTA
NM_004960.4:c.936+148_936+149delinsTA MANE Select NP_004951.1:n.936+148_936+149delinsTA