Canonical Allele Identifier: CA2216944669

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31184981G= , CM000678.2:g.31184981G=	GRCh38
NC_000016.9:g.31196302G= , CM000678.1:g.31196302G=	GRCh37
NC_000016.8:g.31103803G=	NCBI36
NG_012889.2:g.9850G= , LRG_655:g.9850G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.566G= MANE Select	ENSP00000254108.8:p.Gly189=
ENST00000254108.11:c.566G=	ENSP00000254108.7:p.Gly189=
ENST00000380244.7:c.563G=	ENSP00000369594.3:p.Gly188=
ENST00000487509.6:n.631G=
ENST00000566605.5:c.566G=	ENSP00000455073.1:p.Gly189=
ENST00000568685.1:c.566G=	ENSP00000455282.1:p.Gly189=
NM_001170634.1:c.563G=	NP_001164105.1:p.Gly188=
NM_001170937.1:c.554G=	NP_001164408.1:p.Gly185=
NM_004960.3:c.566G= , LRG_655t1:c.566G=	NP_004951.1:p.Gly189=
NR_028388.2:n.671G=
XM_005255233.3:c.-15G=	XP_005255290.1:n.-15G=
XM_011545781.1:c.560G=	XP_011544083.1:p.Gly187=
XM_011545782.1:c.-15G=	XP_011544084.1:n.-15G=
XM_005255233.5:c.-15G=	XP_005255290.1:n.-15G=
XM_011545782.2:c.-15G=	XP_011544084.1:n.-15G=
XM_024450221.1:c.557G=	XP_024305989.1:p.Gly186=
NM_004960.4:c.566G= MANE Select	NP_004951.1:p.Gly189=