Canonical Allele Identifier: CA395666405
Gene: FUS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31183866G>T , CM000678.2:g.31183866G>T GRCh38
NC_000016.9:g.31195187G>T , CM000678.1:g.31195187G>T GRCh37
NC_000016.8:g.31102688G>T NCBI36
NG_012889.2:g.8735G>T , LRG_655:g.8735G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000254108.12:c.199G>T MANE Select ENSP00000254108.8:p.Gly67Ter
ENST00000254108.11:c.199G>T ENSP00000254108.7:p.Gly67Ter
ENST00000380244.7:c.196G>T ENSP00000369594.3:p.Gly66Ter
ENST00000487509.6:n.264G>T
ENST00000487974.1:n.317G>T
ENST00000566605.5:c.199G>T ENSP00000455073.1:p.Gly67Ter
ENST00000568685.1:c.199G>T ENSP00000455282.1:p.Gly67Ter
NM_001170634.1:c.196G>T NP_001164105.1:p.Gly66Ter
NM_001170937.1:c.199G>T NP_001164408.1:p.Gly67Ter
NM_004960.3:c.199G>T , LRG_655t1:c.199G>T NP_004951.1:p.Gly67Ter
NR_028388.2:n.304G>T
XM_005255233.3:c.-382G>T XP_005255290.1:n.-382G>T
XM_011545781.1:c.199G>T XP_011544083.1:p.Gly67Ter
XM_005255233.5:c.-382G>T XP_005255290.1:n.-382G>T
XM_024450221.1:c.196G>T XP_024305989.1:p.Gly66Ter
NM_004960.4:c.199G>T MANE Select NP_004951.1:p.Gly67Ter