Canonical Allele Identifier: CA2216947171

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189169T= , CM000678.2:g.31189169T=	GRCh38
NC_000016.9:g.31200490T= , CM000678.1:g.31200490T=	GRCh37
NC_000016.8:g.31107991T=	NCBI36
NG_012889.2:g.14038T= , LRG_655:g.14038T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.879T= MANE Select	ENSP00000254108.8:p.Gly293=
ENST00000254108.11:c.879T=	ENSP00000254108.7:p.Gly293=
ENST00000380244.7:c.876T=	ENSP00000369594.3:p.Gly292=
ENST00000474990.5:n.173T=
ENST00000487509.6:n.4054T=
ENST00000564766.1:n.703T=
ENST00000566605.5:c.*52T=	ENSP00000455073.1:n.*52T=
ENST00000568685.1:c.882T=	ENSP00000455282.1:p.Gly294=
ENST00000568901.2:n.253T=
NM_001170634.1:c.876T=	NP_001164105.1:p.Gly292=
NM_001170937.1:c.867T=	NP_001164408.1:p.Gly289=
NM_004960.3:c.879T= , LRG_655t1:c.879T=	NP_004951.1:p.Gly293=
NR_028388.2:n.949T=
XM_005255233.3:c.264T=	XP_005255290.1:p.Gly88=
XM_011545781.1:c.873T=	XP_011544083.1:p.Gly291=
XM_011545782.1:c.264T=	XP_011544084.1:p.Gly88=
XM_005255233.5:c.264T=	XP_005255290.1:p.Gly88=
XM_011545782.2:c.264T=	XP_011544084.1:p.Gly88=
XM_024450221.1:c.870T=	XP_024305989.1:p.Gly290=
NM_004960.4:c.879T= MANE Select	NP_004951.1:p.Gly293=