Canonical Allele Identifier: CA976356840
Gene: FUS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31184874A>T , CM000678.2:g.31184874A>T GRCh38
NC_000016.9:g.31196195A>T , CM000678.1:g.31196195A>T GRCh37
NC_000016.8:g.31103696A>T NCBI36
NG_012889.2:g.9743A>T , LRG_655:g.9743A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000254108.12:c.524-65A>T MANE Select ENSP00000254108.8:n.524-65A>T
ENST00000254108.11:c.524-65A>T ENSP00000254108.7:n.524-65A>T
ENST00000380244.7:c.521-65A>T ENSP00000369594.3:n.521-65A>T
ENST00000487509.6:n.589-65A>T
ENST00000566605.5:c.524-65A>T ENSP00000455073.1:n.524-65A>T
ENST00000568685.1:c.524-65A>T ENSP00000455282.1:n.524-65A>T
NM_001170634.1:c.521-65A>T NP_001164105.1:n.521-65A>T
NM_001170937.1:c.512-65A>T NP_001164408.1:n.512-65A>T
NM_004960.3:c.524-65A>T , LRG_655t1:c.524-65A>T NP_004951.1:n.524-65A>T
NR_028388.2:n.629-65A>T
XM_005255233.3:c.-57-65A>T XP_005255290.1:n.-57-65A>T
XM_011545781.1:c.518-65A>T XP_011544083.1:n.518-65A>T
XM_011545782.1:c.-57-65A>T XP_011544084.1:n.-57-65A>T
XM_005255233.5:c.-57-65A>T XP_005255290.1:n.-57-65A>T
XM_011545782.2:c.-57-65A>T XP_011544084.1:n.-57-65A>T
XM_024450221.1:c.515-65A>T XP_024305989.1:n.515-65A>T
NM_004960.4:c.524-65A>T MANE Select NP_004951.1:n.524-65A>T