Canonical Allele Identifier: CA2216947140
Gene: FUS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31189086C= , CM000678.2:g.31189086C= GRCh38
NC_000016.9:g.31200407C= , CM000678.1:g.31200407C= GRCh37
NC_000016.8:g.31107908C= NCBI36
NG_012889.2:g.13955C= , LRG_655:g.13955C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000254108.12:c.833-37C= MANE Select ENSP00000254108.8:n.833-37C=
ENST00000254108.11:c.833-37C= ENSP00000254108.7:n.833-37C=
ENST00000380244.7:c.830-37C= ENSP00000369594.3:n.830-37C=
ENST00000474990.5:n.127-37C=
ENST00000487509.6:n.4008-37C=
ENST00000564766.1:n.620C=
ENST00000566605.5:c.*6-37C= ENSP00000455073.1:n.*6-37C=
ENST00000568685.1:c.833-34C= ENSP00000455282.1:n.833-34C=
ENST00000568901.2:n.207-37C=
NM_001170634.1:c.830-37C= NP_001164105.1:n.830-37C=
NM_001170937.1:c.821-37C= NP_001164408.1:n.821-37C=
NM_004960.3:c.833-37C= , LRG_655t1:c.833-37C= NP_004951.1:n.833-37C=
NR_028388.2:n.903-37C=
XM_005255233.3:c.218-37C= XP_005255290.1:n.218-37C=
XM_011545781.1:c.827-37C= XP_011544083.1:n.827-37C=
XM_011545782.1:c.218-37C= XP_011544084.1:n.218-37C=
XM_005255233.5:c.218-37C= XP_005255290.1:n.218-37C=
XM_011545782.2:c.218-37C= XP_011544084.1:n.218-37C=
XM_024450221.1:c.824-37C= XP_024305989.1:n.824-37C=
NM_004960.4:c.833-37C= MANE Select NP_004951.1:n.833-37C=