Canonical Allele Identifier: CA395666364
Gene: FUS HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000254108.12:c.194G>C MANE Select ENSP00000254108.8:p.Gly65Ala
ENST00000254108.11:c.194G>C ENSP00000254108.7:p.Gly65Ala
ENST00000380244.7:c.191G>C ENSP00000369594.3:p.Ser64Thr
ENST00000487509.6:n.259G>C
ENST00000487974.1:n.312G>C
ENST00000566605.5:c.194G>C ENSP00000455073.1:p.Gly65Ala
ENST00000568685.1:c.194G>C ENSP00000455282.1:p.Gly65Ala
NM_001170634.1:c.191G>C NP_001164105.1:p.Ser64Thr
NM_001170937.1:c.194G>C NP_001164408.1:p.Gly65Ala
NM_004960.3:c.194G>C , LRG_655t1:c.194G>C NP_004951.1:p.Gly65Ala
NR_028388.2:n.299G>C
XM_005255233.3:c.-387G>C XP_005255290.1:n.-387G>C
XM_011545781.1:c.194G>C XP_011544083.1:p.Gly65Ala
XM_005255233.5:c.-387G>C XP_005255290.1:n.-387G>C
XM_024450221.1:c.191G>C XP_024305989.1:p.Ser64Thr
NM_004960.4:c.194G>C MANE Select NP_004951.1:p.Gly65Ala