Canonical Allele Identifier: CA395672313

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31200507A>T (hg19) ; chr16:g.31189186A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189186A>T , CM000678.2:g.31189186A>T	GRCh38
NC_000016.9:g.31200507A>T , CM000678.1:g.31200507A>T	GRCh37
NC_000016.8:g.31108008A>T	NCBI36
NG_012889.2:g.14055A>T , LRG_655:g.14055A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.896A>T MANE Select	ENSP00000254108.8:p.Glu299Val
ENST00000254108.11:c.896A>T	ENSP00000254108.7:p.Glu299Val
ENST00000380244.7:c.893A>T	ENSP00000369594.3:p.Glu298Val
ENST00000474990.5:n.190A>T
ENST00000487509.6:n.4071A>T
ENST00000564766.1:n.720A>T
ENST00000566605.5:c.*69A>T	ENSP00000455073.1:n.*69A>T
ENST00000568685.1:c.899A>T	ENSP00000455282.1:p.Glu300Val
ENST00000568901.2:n.270A>T
NM_001170634.1:c.893A>T	NP_001164105.1:p.Glu298Val
NM_001170937.1:c.884A>T	NP_001164408.1:p.Glu295Val
NM_004960.3:c.896A>T , LRG_655t1:c.896A>T	NP_004951.1:p.Glu299Val
NR_028388.2:n.966A>T
XM_005255233.3:c.281A>T	XP_005255290.1:p.Glu94Val
XM_011545781.1:c.890A>T	XP_011544083.1:p.Glu297Val
XM_011545782.1:c.281A>T	XP_011544084.1:p.Glu94Val
XM_005255233.5:c.281A>T	XP_005255290.1:p.Glu94Val
XM_011545782.2:c.281A>T	XP_011544084.1:p.Glu94Val
XM_024450221.1:c.887A>T	XP_024305989.1:p.Glu296Val
NM_004960.4:c.896A>T MANE Select	NP_004951.1:p.Glu299Val