Canonical Allele Identifier: CA2216942105
Gene: FUS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31183861G= , CM000678.2:g.31183861G= GRCh38
NC_000016.9:g.31195182G= , CM000678.1:g.31195182G= GRCh37
NC_000016.8:g.31102683G= NCBI36
NG_012889.2:g.8730G= , LRG_655:g.8730G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000254108.12:c.194G= MANE Select ENSP00000254108.8:p.Gly65=
ENST00000254108.11:c.194G= ENSP00000254108.7:p.Gly65=
ENST00000380244.7:c.191G= ENSP00000369594.3:p.Ser64=
ENST00000487509.6:n.259G=
ENST00000487974.1:n.312G=
ENST00000566605.5:c.194G= ENSP00000455073.1:p.Gly65=
ENST00000568685.1:c.194G= ENSP00000455282.1:p.Gly65=
NM_001170634.1:c.191G= NP_001164105.1:p.Ser64=
NM_001170937.1:c.194G= NP_001164408.1:p.Gly65=
NM_004960.3:c.194G= , LRG_655t1:c.194G= NP_004951.1:p.Gly65=
NR_028388.2:n.299G=
XM_005255233.3:c.-387G= XP_005255290.1:n.-387G=
XM_011545781.1:c.194G= XP_011544083.1:p.Gly65=
XM_005255233.5:c.-387G= XP_005255290.1:n.-387G=
XM_024450221.1:c.191G= XP_024305989.1:p.Ser64=
NM_004960.4:c.194G= MANE Select NP_004951.1:p.Gly65=