Canonical Allele Identifier: CA2732100305
Gene: FUS HGNC NCBI

Linked Data

dbSNP Id: rs2144143153

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31191518T>A , CM000678.2:g.31191518T>A GRCh38
NC_000016.9:g.31202839T>A , CM000678.1:g.31202839T>A GRCh37
NC_000016.8:g.31110340T>A NCBI36
NG_012889.2:g.16387T>A , LRG_655:g.16387T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000254108.12:c.*80T>A MANE Select ENSP00000254108.8:n.*80T>A
ENST00000254108.11:c.*80T>A ENSP00000254108.7:n.*80T>A
ENST00000380244.7:c.*80T>A ENSP00000369594.3:n.*80T>A
ENST00000483853.1:n.738T>A
ENST00000487509.6:n.4836T>A
ENST00000566605.5:c.*834T>A ENSP00000455073.1:n.*834T>A
ENST00000568685.1:c.*80T>A ENSP00000455282.1:n.*80T>A
ENST00000569760.5:n.552T>A
NM_001170634.1:c.*80T>A NP_001164105.1:n.*80T>A
NM_001170937.1:c.*80T>A NP_001164408.1:n.*80T>A
NM_004960.3:c.*80T>A , LRG_655t1:c.*80T>A NP_004951.1:n.*80T>A
NR_028388.2:n.1731T>A
XM_005255233.3:c.*80T>A XP_005255290.1:n.*80T>A
XM_011545781.1:c.*80T>A XP_011544083.1:n.*80T>A
XM_011545782.1:c.*80T>A XP_011544084.1:n.*80T>A
XM_005255233.5:c.*80T>A XP_005255290.1:n.*80T>A
XM_011545782.2:c.*80T>A XP_011544084.1:n.*80T>A
XM_024450221.1:c.*80T>A XP_024305989.1:n.*80T>A
NM_004960.4:c.*80T>A MANE Select NP_004951.1:n.*80T>A