Canonical Allele Identifier: CA2216942349

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31183963G= , CM000678.2:g.31183963G=	GRCh38
NC_000016.9:g.31195284G= , CM000678.1:g.31195284G=	GRCh37
NC_000016.8:g.31102785G=	NCBI36
NG_012889.2:g.8832G= , LRG_655:g.8832G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.296G= MANE Select	ENSP00000254108.8:p.Gly99=
ENST00000254108.11:c.296G=	ENSP00000254108.7:p.Gly99=
ENST00000380244.7:c.293G=	ENSP00000369594.3:p.Gly98=
ENST00000487509.6:n.361G=
ENST00000487974.1:n.414G=
ENST00000566605.5:c.296G=	ENSP00000455073.1:p.Gly99=
ENST00000568685.1:c.296G=	ENSP00000455282.1:p.Gly99=
NM_001170634.1:c.293G=	NP_001164105.1:p.Gly98=
NM_001170937.1:c.296G=	NP_001164408.1:p.Gly99=
NM_004960.3:c.296G= , LRG_655t1:c.296G=	NP_004951.1:p.Gly99=
NR_028388.2:n.401G=
XM_005255233.3:c.-285G=	XP_005255290.1:n.-285G=
XM_011545781.1:c.296G=	XP_011544083.1:p.Gly99=
XM_005255233.5:c.-285G=	XP_005255290.1:n.-285G=
XM_024450221.1:c.293G=	XP_024305989.1:p.Gly98=
NM_004960.4:c.296G= MANE Select	NP_004951.1:p.Gly99=