Canonical Allele Identifier: CA2216948383

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31191427A= , CM000678.2:g.31191427A=	GRCh38
NC_000016.9:g.31202748A= , CM000678.1:g.31202748A=	GRCh37
NC_000016.8:g.31110249A=	NCBI36
NG_012889.2:g.16296A= , LRG_655:g.16296A=

Transcript Alleles

HGVS	Amino-acid Change
NM_004960.4:c.1570A= MANE Select	NP_004951.1:p.Arg524=
ENST00000254108.12:c.1570A= MANE Select	ENSP00000254108.8:p.Arg524=
NM_001170634.1:c.1567A=	NP_001164105.1:p.Arg523=
NM_001170937.1:c.1558A=	NP_001164408.1:p.Arg520=
NM_004960.3:c.1570A= , LRG_655t1:c.1570A=	NP_004951.1:p.Arg524=
NR_028388.2:n.1640A=
ENST00000254108.11:c.1570A=	ENSP00000254108.7:p.Arg524=
ENST00000380244.7:c.1567A=	ENSP00000369594.3:p.Arg523=
ENST00000483853.1:n.647A=
ENST00000487509.6:n.4745A=
ENST00000566605.5:c.*743A=	ENSP00000455073.1:n.*743A=
ENST00000568685.1:c.1573A=	ENSP00000455282.1:p.Arg525=
ENST00000569760.5:n.461A=
XM_005255233.3:c.955A=	XP_005255290.1:p.Arg319=
XM_005255233.5:c.955A=	XP_005255290.1:p.Arg319=
XM_011545781.1:c.1564A=	XP_011544083.1:p.Arg522=
XM_011545782.1:c.955A=	XP_011544084.1:p.Arg319=
XM_011545782.2:c.955A=	XP_011544084.1:p.Arg319=
XM_024450221.1:c.1561A=	XP_024305989.1:p.Arg521=