Canonical Allele Identifier: CA2632839868
Gene: FUS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31189050A>T , CM000678.2:g.31189050A>T GRCh38
NC_000016.9:g.31200371A>T , CM000678.1:g.31200371A>T GRCh37
NC_000016.8:g.31107872A>T NCBI36
NG_012889.2:g.13919A>T , LRG_655:g.13919A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000254108.12:c.833-73A>T MANE Select ENSP00000254108.8:n.833-73A>T
ENST00000254108.11:c.833-73A>T ENSP00000254108.7:n.833-73A>T
ENST00000380244.7:c.830-73A>T ENSP00000369594.3:n.830-73A>T
ENST00000474990.5:n.127-73A>T
ENST00000487509.6:n.4008-73A>T
ENST00000564766.1:n.584A>T
ENST00000566605.5:c.*6-73A>T ENSP00000455073.1:n.*6-73A>T
ENST00000568685.1:c.833-70A>T ENSP00000455282.1:n.833-70A>T
ENST00000568901.2:n.207-73A>T
NM_001170634.1:c.830-73A>T NP_001164105.1:n.830-73A>T
NM_001170937.1:c.821-73A>T NP_001164408.1:n.821-73A>T
NM_004960.3:c.833-73A>T , LRG_655t1:c.833-73A>T NP_004951.1:n.833-73A>T
NR_028388.2:n.903-73A>T
XM_005255233.3:c.218-73A>T XP_005255290.1:n.218-73A>T
XM_011545781.1:c.827-73A>T XP_011544083.1:n.827-73A>T
XM_011545782.1:c.218-73A>T XP_011544084.1:n.218-73A>T
XM_005255233.5:c.218-73A>T XP_005255290.1:n.218-73A>T
XM_011545782.2:c.218-73A>T XP_011544084.1:n.218-73A>T
XM_024450221.1:c.824-73A>T XP_024305989.1:n.824-73A>T
NM_004960.4:c.833-73A>T MANE Select NP_004951.1:n.833-73A>T