Canonical Allele Identifier: CA976359459
Gene: FUS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31189077_31189079del , CM000678.2:g.31189077_31189079del GRCh38
NC_000016.9:g.31200398_31200400del , CM000678.1:g.31200398_31200400del GRCh37
NC_000016.8:g.31107899_31107901del NCBI36
NG_012889.2:g.13946_13948del , LRG_655:g.13946_13948del

Transcript Alleles

HGVS Amino-acid Change
ENST00000254108.12:c.833-46_833-44del MANE Select ENSP00000254108.8:n.833-46_833-44del
ENST00000254108.11:c.833-46_833-44del ENSP00000254108.7:n.833-46_833-44del
ENST00000380244.7:c.830-46_830-44del ENSP00000369594.3:n.830-46_830-44del
ENST00000474990.5:n.127-46_127-44del
ENST00000487509.6:n.4008-46_4008-44del
ENST00000564766.1:n.611_613del
ENST00000566605.5:c.*6-46_*6-44del ENSP00000455073.1:n.*6-46_*6-44del
ENST00000568685.1:c.833-43_833-41del ENSP00000455282.1:n.833-43_833-41del
ENST00000568901.2:n.207-46_207-44del
NM_001170634.1:c.830-46_830-44del NP_001164105.1:n.830-46_830-44del
NM_001170937.1:c.821-46_821-44del NP_001164408.1:n.821-46_821-44del
NM_004960.3:c.833-46_833-44del , LRG_655t1:c.833-46_833-44del NP_004951.1:n.833-46_833-44del
NR_028388.2:n.903-46_903-44del
XM_005255233.3:c.218-46_218-44del XP_005255290.1:n.218-46_218-44del
XM_011545781.1:c.827-46_827-44del XP_011544083.1:n.827-46_827-44del
XM_011545782.1:c.218-46_218-44del XP_011544084.1:n.218-46_218-44del
XM_005255233.5:c.218-46_218-44del XP_005255290.1:n.218-46_218-44del
XM_011545782.2:c.218-46_218-44del XP_011544084.1:n.218-46_218-44del
XM_024450221.1:c.824-46_824-44del XP_024305989.1:n.824-46_824-44del
NM_004960.4:c.833-46_833-44del MANE Select NP_004951.1:n.833-46_833-44del