Canonical Allele Identifier: CA395672329
Gene: FUS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31189189C>G , CM000678.2:g.31189189C>G GRCh38
NC_000016.9:g.31200510C>G , CM000678.1:g.31200510C>G GRCh37
NC_000016.8:g.31108011C>G NCBI36
NG_012889.2:g.14058C>G , LRG_655:g.14058C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000254108.12:c.899C>G MANE Select ENSP00000254108.8:p.Ser300Cys
ENST00000254108.11:c.899C>G ENSP00000254108.7:p.Ser300Cys
ENST00000380244.7:c.896C>G ENSP00000369594.3:p.Ser299Cys
ENST00000474990.5:n.193C>G
ENST00000487509.6:n.4074C>G
ENST00000564766.1:n.723C>G
ENST00000566605.5:c.*72C>G ENSP00000455073.1:n.*72C>G
ENST00000568685.1:c.902C>G ENSP00000455282.1:p.Ser301Cys
ENST00000568901.2:n.273C>G
NM_001170634.1:c.896C>G NP_001164105.1:p.Ser299Cys
NM_001170937.1:c.887C>G NP_001164408.1:p.Ser296Cys
NM_004960.3:c.899C>G , LRG_655t1:c.899C>G NP_004951.1:p.Ser300Cys
NR_028388.2:n.969C>G
XM_005255233.3:c.284C>G XP_005255290.1:p.Ser95Cys
XM_011545781.1:c.893C>G XP_011544083.1:p.Ser298Cys
XM_011545782.1:c.284C>G XP_011544084.1:p.Ser95Cys
XM_005255233.5:c.284C>G XP_005255290.1:p.Ser95Cys
XM_011545782.2:c.284C>G XP_011544084.1:p.Ser95Cys
XM_024450221.1:c.890C>G XP_024305989.1:p.Ser297Cys
NM_004960.4:c.899C>G MANE Select NP_004951.1:p.Ser300Cys