Canonical Allele Identifier: CA2216947178

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189197G= , CM000678.2:g.31189197G=	GRCh38
NC_000016.9:g.31200518G= , CM000678.1:g.31200518G=	GRCh37
NC_000016.8:g.31108019G=	NCBI36
NG_012889.2:g.14066G= , LRG_655:g.14066G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.907G= MANE Select	ENSP00000254108.8:p.Asp303=
ENST00000254108.11:c.907G=	ENSP00000254108.7:p.Asp303=
ENST00000380244.7:c.904G=	ENSP00000369594.3:p.Asp302=
ENST00000474990.5:n.201G=
ENST00000487509.6:n.4082G=
ENST00000564766.1:n.731G=
ENST00000566605.5:c.*80G=	ENSP00000455073.1:n.*80G=
ENST00000568685.1:c.910G=	ENSP00000455282.1:p.Asp304=
ENST00000568901.2:n.281G=
NM_001170634.1:c.904G=	NP_001164105.1:p.Asp302=
NM_001170937.1:c.895G=	NP_001164408.1:p.Asp299=
NM_004960.3:c.907G= , LRG_655t1:c.907G=	NP_004951.1:p.Asp303=
NR_028388.2:n.977G=
XM_005255233.3:c.292G=	XP_005255290.1:p.Asp98=
XM_011545781.1:c.901G=	XP_011544083.1:p.Asp301=
XM_011545782.1:c.292G=	XP_011544084.1:p.Asp98=
XM_005255233.5:c.292G=	XP_005255290.1:p.Asp98=
XM_011545782.2:c.292G=	XP_011544084.1:p.Asp98=
XM_024450221.1:c.898G=	XP_024305989.1:p.Asp300=
NM_004960.4:c.907G= MANE Select	NP_004951.1:p.Asp303=