Canonical Allele Identifier: CA2216948375

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31191412C= , CM000678.2:g.31191412C=	GRCh38
NC_000016.9:g.31202733C= , CM000678.1:g.31202733C=	GRCh37
NC_000016.8:g.31110234C=	NCBI36
NG_012889.2:g.16281C= , LRG_655:g.16281C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000254108.12:c.1555C= MANE Select	ENSP00000254108.8:p.Gln519=
ENST00000254108.11:c.1555C=	ENSP00000254108.7:p.Gln519=
ENST00000380244.7:c.1552C=	ENSP00000369594.3:p.Gln518=
ENST00000483853.1:n.632C=
ENST00000487509.6:n.4730C=
ENST00000566605.5:c.*728C=	ENSP00000455073.1:n.*728C=
ENST00000568685.1:c.1558C=	ENSP00000455282.1:p.Gln520=
ENST00000569760.5:n.446C=
NM_001170634.1:c.1552C=	NP_001164105.1:p.Gln518=
NM_001170937.1:c.1543C=	NP_001164408.1:p.Gln515=
NM_004960.3:c.1555C= , LRG_655t1:c.1555C=	NP_004951.1:p.Gln519=
NR_028388.2:n.1625C=
XM_005255233.3:c.940C=	XP_005255290.1:p.Gln314=
XM_011545781.1:c.1549C=	XP_011544083.1:p.Gln517=
XM_011545782.1:c.940C=	XP_011544084.1:p.Gln314=
XM_005255233.5:c.940C=	XP_005255290.1:p.Gln314=
XM_011545782.2:c.940C=	XP_011544084.1:p.Gln314=
XM_024450221.1:c.1546C=	XP_024305989.1:p.Gln516=
NM_004960.4:c.1555C= MANE Select	NP_004951.1:p.Gln519=