Canonical Allele Identifier: CA2216907476

Gene: FUS

Genomic Alleles

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

Transcript Alleles

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