Canonical Allele Identifier: CA2216944642

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31184960C= , CM000678.2:g.31184960C=	GRCh38
NC_000016.9:g.31196281C= , CM000678.1:g.31196281C=	GRCh37
NC_000016.8:g.31103782C=	NCBI36
NG_012889.2:g.9829C= , LRG_655:g.9829C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.545C= MANE Select	ENSP00000254108.8:p.Ser182=
ENST00000254108.11:c.545C=	ENSP00000254108.7:p.Ser182=
ENST00000380244.7:c.542C=	ENSP00000369594.3:p.Ser181=
ENST00000487509.6:n.610C=
ENST00000566605.5:c.545C=	ENSP00000455073.1:p.Ser182=
ENST00000568685.1:c.545C=	ENSP00000455282.1:p.Ser182=
NM_001170634.1:c.542C=	NP_001164105.1:p.Ser181=
NM_001170937.1:c.533C=	NP_001164408.1:p.Ser178=
NM_004960.3:c.545C= , LRG_655t1:c.545C=	NP_004951.1:p.Ser182=
NR_028388.2:n.650C=
XM_005255233.3:c.-36C=	XP_005255290.1:n.-36C=
XM_011545781.1:c.539C=	XP_011544083.1:p.Ser180=
XM_011545782.1:c.-36C=	XP_011544084.1:n.-36C=
XM_005255233.5:c.-36C=	XP_005255290.1:n.-36C=
XM_011545782.2:c.-36C=	XP_011544084.1:n.-36C=
XM_024450221.1:c.536C=	XP_024305989.1:p.Ser179=
NM_004960.4:c.545C= MANE Select	NP_004951.1:p.Ser182=