Canonical Allele Identifier: CA2216948377

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31191419G= , CM000678.2:g.31191419G=	GRCh38
NC_000016.9:g.31202740G= , CM000678.1:g.31202740G=	GRCh37
NC_000016.8:g.31110241G=	NCBI36
NG_012889.2:g.16288G= , LRG_655:g.16288G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000254108.12:c.1562G= MANE Select	ENSP00000254108.8:p.Arg521=
ENST00000254108.11:c.1562G=	ENSP00000254108.7:p.Arg521=
ENST00000380244.7:c.1559G=	ENSP00000369594.3:p.Arg520=
ENST00000483853.1:n.639G=
ENST00000487509.6:n.4737G=
ENST00000566605.5:c.*735G=	ENSP00000455073.1:n.*735G=
ENST00000568685.1:c.1565G=	ENSP00000455282.1:p.Arg522=
ENST00000569760.5:n.453G=
NM_001170634.1:c.1559G=	NP_001164105.1:p.Arg520=
NM_001170937.1:c.1550G=	NP_001164408.1:p.Arg517=
NM_004960.3:c.1562G= , LRG_655t1:c.1562G=	NP_004951.1:p.Arg521=
NR_028388.2:n.1632G=
XM_005255233.3:c.947G=	XP_005255290.1:p.Arg316=
XM_011545781.1:c.1556G=	XP_011544083.1:p.Arg519=
XM_011545782.1:c.947G=	XP_011544084.1:p.Arg316=
XM_005255233.5:c.947G=	XP_005255290.1:p.Arg316=
XM_011545782.2:c.947G=	XP_011544084.1:p.Arg316=
XM_024450221.1:c.1553G=	XP_024305989.1:p.Arg518=
NM_004960.4:c.1562G= MANE Select	NP_004951.1:p.Arg521=