Canonical Allele Identifier: CA2216944691

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31184988T= , CM000678.2:g.31184988T=	GRCh38
NC_000016.9:g.31196309T= , CM000678.1:g.31196309T=	GRCh37
NC_000016.8:g.31103810T=	NCBI36
NG_012889.2:g.9857T= , LRG_655:g.9857T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.573T= MANE Select	ENSP00000254108.8:p.Gly191=
ENST00000254108.11:c.573T=	ENSP00000254108.7:p.Gly191=
ENST00000380244.7:c.570T=	ENSP00000369594.3:p.Gly190=
ENST00000487509.6:n.638T=
ENST00000566605.5:c.573T=	ENSP00000455073.1:p.Gly191=
ENST00000568685.1:c.573T=	ENSP00000455282.1:p.Gly191=
NM_001170634.1:c.570T=	NP_001164105.1:p.Gly190=
NM_001170937.1:c.561T=	NP_001164408.1:p.Gly187=
NM_004960.3:c.573T= , LRG_655t1:c.573T=	NP_004951.1:p.Gly191=
NR_028388.2:n.678T=
XM_005255233.3:c.-8T=	XP_005255290.1:n.-8T=
XM_011545781.1:c.567T=	XP_011544083.1:p.Gly189=
XM_011545782.1:c.-8T=	XP_011544084.1:n.-8T=
XM_005255233.5:c.-8T=	XP_005255290.1:n.-8T=
XM_011545782.2:c.-8T=	XP_011544084.1:n.-8T=
XM_024450221.1:c.564T=	XP_024305989.1:p.Gly188=
NM_004960.4:c.573T= MANE Select	NP_004951.1:p.Gly191=