Canonical Allele Identifier: CA2216944196
Gene: FUS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31184845A= , CM000678.2:g.31184845A= GRCh38
NC_000016.9:g.31196166A= , CM000678.1:g.31196166A= GRCh37
NC_000016.8:g.31103667A= NCBI36
NG_012889.2:g.9714A= , LRG_655:g.9714A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000254108.12:c.524-94A= MANE Select ENSP00000254108.8:n.524-94A=
ENST00000254108.11:c.524-94A= ENSP00000254108.7:n.524-94A=
ENST00000380244.7:c.521-94A= ENSP00000369594.3:n.521-94A=
ENST00000487509.6:n.589-94A=
ENST00000566605.5:c.524-94A= ENSP00000455073.1:n.524-94A=
ENST00000568685.1:c.524-94A= ENSP00000455282.1:n.524-94A=
NM_001170634.1:c.521-94A= NP_001164105.1:n.521-94A=
NM_001170937.1:c.512-94A= NP_001164408.1:n.512-94A=
NM_004960.3:c.524-94A= , LRG_655t1:c.524-94A= NP_004951.1:n.524-94A=
NR_028388.2:n.629-94A=
XM_005255233.3:c.-57-94A= XP_005255290.1:n.-57-94A=
XM_011545781.1:c.518-94A= XP_011544083.1:n.518-94A=
XM_011545782.1:c.-57-94A= XP_011544084.1:n.-57-94A=
XM_005255233.5:c.-57-94A= XP_005255290.1:n.-57-94A=
XM_011545782.2:c.-57-94A= XP_011544084.1:n.-57-94A=
XM_024450221.1:c.515-94A= XP_024305989.1:n.515-94A=
NM_004960.4:c.524-94A= MANE Select NP_004951.1:n.524-94A=