Canonical Allele Identifier: CA2216947168

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189158C= , CM000678.2:g.31189158C=	GRCh38
NC_000016.9:g.31200479C= , CM000678.1:g.31200479C=	GRCh37
NC_000016.8:g.31107980C=	NCBI36
NG_012889.2:g.14027C= , LRG_655:g.14027C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.868C= MANE Select	ENSP00000254108.8:p.Gln290=
ENST00000254108.11:c.868C=	ENSP00000254108.7:p.Gln290=
ENST00000380244.7:c.865C=	ENSP00000369594.3:p.Gln289=
ENST00000474990.5:n.162C=
ENST00000487509.6:n.4043C=
ENST00000564766.1:n.692C=
ENST00000566605.5:c.*41C=	ENSP00000455073.1:n.*41C=
ENST00000568685.1:c.871C=	ENSP00000455282.1:p.Gln291=
ENST00000568901.2:n.242C=
NM_001170634.1:c.865C=	NP_001164105.1:p.Gln289=
NM_001170937.1:c.856C=	NP_001164408.1:p.Gln286=
NM_004960.3:c.868C= , LRG_655t1:c.868C=	NP_004951.1:p.Gln290=
NR_028388.2:n.938C=
XM_005255233.3:c.253C=	XP_005255290.1:p.Gln85=
XM_011545781.1:c.862C=	XP_011544083.1:p.Gln288=
XM_011545782.1:c.253C=	XP_011544084.1:p.Gln85=
XM_005255233.5:c.253C=	XP_005255290.1:p.Gln85=
XM_011545782.2:c.253C=	XP_011544084.1:p.Gln85=
XM_024450221.1:c.859C=	XP_024305989.1:p.Gln287=
NM_004960.4:c.868C= MANE Select	NP_004951.1:p.Gln290=