Canonical Allele Identifier: CA395672231
Gene: FUS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31189174A>C , CM000678.2:g.31189174A>C GRCh38
NC_000016.9:g.31200495A>C , CM000678.1:g.31200495A>C GRCh37
NC_000016.8:g.31107996A>C NCBI36
NG_012889.2:g.14043A>C , LRG_655:g.14043A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000254108.12:c.884A>C MANE Select ENSP00000254108.8:p.Asn295Thr
ENST00000254108.11:c.884A>C ENSP00000254108.7:p.Asn295Thr
ENST00000380244.7:c.881A>C ENSP00000369594.3:p.Asn294Thr
ENST00000474990.5:n.178A>C
ENST00000487509.6:n.4059A>C
ENST00000564766.1:n.708A>C
ENST00000566605.5:c.*57A>C ENSP00000455073.1:n.*57A>C
ENST00000568685.1:c.887A>C ENSP00000455282.1:p.Asn296Thr
ENST00000568901.2:n.258A>C
NM_001170634.1:c.881A>C NP_001164105.1:p.Asn294Thr
NM_001170937.1:c.872A>C NP_001164408.1:p.Asn291Thr
NM_004960.3:c.884A>C , LRG_655t1:c.884A>C NP_004951.1:p.Asn295Thr
NR_028388.2:n.954A>C
XM_005255233.3:c.269A>C XP_005255290.1:p.Asn90Thr
XM_011545781.1:c.878A>C XP_011544083.1:p.Asn293Thr
XM_011545782.1:c.269A>C XP_011544084.1:p.Asn90Thr
XM_005255233.5:c.269A>C XP_005255290.1:p.Asn90Thr
XM_011545782.2:c.269A>C XP_011544084.1:p.Asn90Thr
XM_024450221.1:c.875A>C XP_024305989.1:p.Asn292Thr
NM_004960.4:c.884A>C MANE Select NP_004951.1:p.Asn295Thr