Canonical Allele Identifier: CA2216948142

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31191052C= , CM000678.2:g.31191052C=	GRCh38
NC_000016.9:g.31202373C= , CM000678.1:g.31202373C=	GRCh37
NC_000016.8:g.31109874C=	NCBI36
NG_012889.2:g.15921C= , LRG_655:g.15921C=

Transcript Alleles

HGVS	Amino-acid Change
NM_004960.4:c.1483C= MANE Select	NP_004951.1:p.Arg495=
ENST00000254108.12:c.1483C= MANE Select	ENSP00000254108.8:p.Arg495=
NM_001170634.1:c.1480C=	NP_001164105.1:p.Arg494=
NM_001170937.1:c.1471C=	NP_001164408.1:p.Arg491=
NM_004960.3:c.1483C= , LRG_655t1:c.1483C=	NP_004951.1:p.Arg495=
NR_028388.2:n.1553C=
ENST00000254108.11:c.1483C=	ENSP00000254108.7:p.Arg495=
ENST00000380244.7:c.1480C=	ENSP00000369594.3:p.Arg494=
ENST00000474990.5:n.777C=
ENST00000483853.1:n.560C=
ENST00000487509.6:n.4658C=
ENST00000566605.5:c.*656C=	ENSP00000455073.1:n.*656C=
ENST00000568685.1:c.1486C=	ENSP00000455282.1:p.Arg496=
ENST00000569760.5:n.374C=
XM_005255233.3:c.868C=	XP_005255290.1:p.Arg290=
XM_005255233.5:c.868C=	XP_005255290.1:p.Arg290=
XM_011545781.1:c.1477C=	XP_011544083.1:p.Arg493=
XM_011545782.1:c.868C=	XP_011544084.1:p.Arg290=
XM_011545782.2:c.868C=	XP_011544084.1:p.Arg290=
XM_024450221.1:c.1474C=	XP_024305989.1:p.Arg492=