Canonical Allele Identifier: CA2632840396

Gene: FUS

Linked Data

• gnomAD v4: 16-31191516-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31191516A>G , CM000678.2:g.31191516A>G	GRCh38
NC_000016.9:g.31202837A>G , CM000678.1:g.31202837A>G	GRCh37
NC_000016.8:g.31110338A>G	NCBI36
NG_012889.2:g.16385A>G , LRG_655:g.16385A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.*78A>G MANE Select	ENSP00000254108.8:n.*78A>G
ENST00000254108.11:c.*78A>G	ENSP00000254108.7:n.*78A>G
ENST00000380244.7:c.*78A>G	ENSP00000369594.3:n.*78A>G
ENST00000483853.1:n.736A>G
ENST00000487509.6:n.4834A>G
ENST00000566605.5:c.*832A>G	ENSP00000455073.1:n.*832A>G
ENST00000568685.1:c.*78A>G	ENSP00000455282.1:n.*78A>G
ENST00000569760.5:n.550A>G
NM_001170634.1:c.*78A>G	NP_001164105.1:n.*78A>G
NM_001170937.1:c.*78A>G	NP_001164408.1:n.*78A>G
NM_004960.3:c.*78A>G , LRG_655t1:c.*78A>G	NP_004951.1:n.*78A>G
NR_028388.2:n.1729A>G
XM_005255233.3:c.*78A>G	XP_005255290.1:n.*78A>G
XM_011545781.1:c.*78A>G	XP_011544083.1:n.*78A>G
XM_011545782.1:c.*78A>G	XP_011544084.1:n.*78A>G
XM_005255233.5:c.*78A>G	XP_005255290.1:n.*78A>G
XM_011545782.2:c.*78A>G	XP_011544084.1:n.*78A>G
XM_024450221.1:c.*78A>G	XP_024305989.1:n.*78A>G
NM_004960.4:c.*78A>G MANE Select	NP_004951.1:n.*78A>G