Canonical Allele Identifier: CA2216944828

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31185049G= , CM000678.2:g.31185049G=	GRCh38
NC_000016.9:g.31196370G= , CM000678.1:g.31196370G=	GRCh37
NC_000016.8:g.31103871G=	NCBI36
NG_012889.2:g.9918G= , LRG_655:g.9918G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.634G= MANE Select	ENSP00000254108.8:p.Asp212=
ENST00000254108.11:c.634G=	ENSP00000254108.7:p.Asp212=
ENST00000380244.7:c.631G=	ENSP00000369594.3:p.Asp211=
ENST00000487509.6:n.699G=
ENST00000566605.5:c.634G=	ENSP00000455073.1:p.Asp212=
ENST00000568685.1:c.634G=	ENSP00000455282.1:p.Asp212=
NM_001170634.1:c.631G=	NP_001164105.1:p.Asp211=
NM_001170937.1:c.622G=	NP_001164408.1:p.Asp208=
NM_004960.3:c.634G= , LRG_655t1:c.634G=	NP_004951.1:p.Asp212=
NR_028388.2:n.739G=
XM_005255233.3:c.54G=	XP_005255290.1:p.Arg18=
XM_011545781.1:c.628G=	XP_011544083.1:p.Asp210=
XM_011545782.1:c.54G=	XP_011544084.1:p.Arg18=
XM_005255233.5:c.54G=	XP_005255290.1:p.Arg18=
XM_011545782.2:c.54G=	XP_011544084.1:p.Arg18=
XM_024450221.1:c.625G=	XP_024305989.1:p.Asp209=
NM_004960.4:c.634G= MANE Select	NP_004951.1:p.Asp212=