Canonical Allele Identifier: CA494713649

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31200481A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189160A>G , CM000678.2:g.31189160A>G	GRCh38
NC_000016.9:g.31200481A>G , CM000678.1:g.31200481A>G	GRCh37
NC_000016.8:g.31107982A>G	NCBI36
NG_012889.2:g.14029A>G , LRG_655:g.14029A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.870A>G MANE Select	ENSP00000254108.8:p.Gln290=
ENST00000254108.11:c.870A>G	ENSP00000254108.7:p.Gln290=
ENST00000380244.7:c.867A>G	ENSP00000369594.3:p.Gln289=
ENST00000474990.5:n.164A>G
ENST00000487509.6:n.4045A>G
ENST00000564766.1:n.694A>G
ENST00000566605.5:c.*43A>G	ENSP00000455073.1:n.*43A>G
ENST00000568685.1:c.873A>G	ENSP00000455282.1:p.Gln291=
ENST00000568901.2:n.244A>G
NM_001170634.1:c.867A>G	NP_001164105.1:p.Gln289=
NM_001170937.1:c.858A>G	NP_001164408.1:p.Gln286=
NM_004960.3:c.870A>G , LRG_655t1:c.870A>G	NP_004951.1:p.Gln290=
NR_028388.2:n.940A>G
XM_005255233.3:c.255A>G	XP_005255290.1:p.Gln85=
XM_011545781.1:c.864A>G	XP_011544083.1:p.Gln288=
XM_011545782.1:c.255A>G	XP_011544084.1:p.Gln85=
XM_005255233.5:c.255A>G	XP_005255290.1:p.Gln85=
XM_011545782.2:c.255A>G	XP_011544084.1:p.Gln85=
XM_024450221.1:c.861A>G	XP_024305989.1:p.Gln287=
NM_004960.4:c.870A>G MANE Select	NP_004951.1:p.Gln290=