Canonical Allele Identifier: CA8024148

Gene: FUS

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31191548G>T , CM000678.2:g.31191548G>T	GRCh38
NC_000016.9:g.31202869G>T , CM000678.1:g.31202869G>T	GRCh37
NC_000016.8:g.31110370G>T	NCBI36
NG_012889.2:g.16417G>T , LRG_655:g.16417G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.*110G>T MANE Select	ENSP00000254108.8:n.*110G>T
ENST00000254108.11:c.*110G>T	ENSP00000254108.7:n.*110G>T
ENST00000380244.7:c.*110G>T	ENSP00000369594.3:n.*110G>T
ENST00000483853.1:n.768G>T
ENST00000487509.6:n.4866G>T
ENST00000566605.5:c.*864G>T	ENSP00000455073.1:n.*864G>T
ENST00000568685.1:c.*110G>T	ENSP00000455282.1:n.*110G>T
ENST00000569760.5:n.582G>T
NM_001170634.1:c.*110G>T	NP_001164105.1:n.*110G>T
NM_001170937.1:c.*110G>T	NP_001164408.1:n.*110G>T
NM_004960.3:c.*110G>T , LRG_655t1:c.*110G>T	NP_004951.1:n.*110G>T
NR_028388.2:n.1761G>T
XM_005255233.3:c.*110G>T	XP_005255290.1:n.*110G>T
XM_011545781.1:c.*110G>T	XP_011544083.1:n.*110G>T
XM_011545782.1:c.*110G>T	XP_011544084.1:n.*110G>T
XM_005255233.5:c.*110G>T	XP_005255290.1:n.*110G>T
XM_011545782.2:c.*110G>T	XP_011544084.1:n.*110G>T
XM_024450221.1:c.*110G>T	XP_024305989.1:n.*110G>T
NM_004960.4:c.*110G>T MANE Select	NP_004951.1:n.*110G>T