Canonical Allele Identifier: CA2216947134
Gene: FUS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31189076T= , CM000678.2:g.31189076T= GRCh38
NC_000016.9:g.31200397T= , CM000678.1:g.31200397T= GRCh37
NC_000016.8:g.31107898T= NCBI36
NG_012889.2:g.13945T= , LRG_655:g.13945T=

Transcript Alleles

HGVS Amino-acid change
ENST00000254108.12:c.833-47T= MANE Select ENSP00000254108.8:n.833-47T=
ENST00000254108.11:c.833-47T= ENSP00000254108.7:n.833-47T=
ENST00000380244.7:c.830-47T= ENSP00000369594.3:n.830-47T=
ENST00000474990.5:n.127-47T=
ENST00000487509.6:n.4008-47T=
ENST00000564766.1:n.610T=
ENST00000566605.5:c.*6-47T= ENSP00000455073.1:n.*6-47T=
ENST00000568685.1:c.833-44T= ENSP00000455282.1:n.833-44T=
ENST00000568901.2:n.207-47T=
NM_001170634.1:c.830-47T= NP_001164105.1:n.830-47T=
NM_001170937.1:c.821-47T= NP_001164408.1:n.821-47T=
NM_004960.3:c.833-47T= , LRG_655t1:c.833-47T= NP_004951.1:n.833-47T=
NR_028388.2:n.903-47T=
XM_005255233.3:c.218-47T= XP_005255290.1:n.218-47T=
XM_011545781.1:c.827-47T= XP_011544083.1:n.827-47T=
XM_011545782.1:c.218-47T= XP_011544084.1:n.218-47T=
XM_005255233.5:c.218-47T= XP_005255290.1:n.218-47T=
XM_011545782.2:c.218-47T= XP_011544084.1:n.218-47T=
XM_024450221.1:c.824-47T= XP_024305989.1:n.824-47T=
NM_004960.4:c.833-47T= MANE Select NP_004951.1:n.833-47T=