Canonical Allele Identifier: CA395672278

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31200501C>G (hg19) ; chr16:g.31189180C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189180C>G , CM000678.2:g.31189180C>G	GRCh38
NC_000016.9:g.31200501C>G , CM000678.1:g.31200501C>G	GRCh37
NC_000016.8:g.31108002C>G	NCBI36
NG_012889.2:g.14049C>G , LRG_655:g.14049C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.890C>G MANE Select	ENSP00000254108.8:p.Thr297Arg
ENST00000254108.11:c.890C>G	ENSP00000254108.7:p.Thr297Arg
ENST00000380244.7:c.887C>G	ENSP00000369594.3:p.Thr296Arg
ENST00000474990.5:n.184C>G
ENST00000487509.6:n.4065C>G
ENST00000564766.1:n.714C>G
ENST00000566605.5:c.*63C>G	ENSP00000455073.1:n.*63C>G
ENST00000568685.1:c.893C>G	ENSP00000455282.1:p.Thr298Arg
ENST00000568901.2:n.264C>G
NM_001170634.1:c.887C>G	NP_001164105.1:p.Thr296Arg
NM_001170937.1:c.878C>G	NP_001164408.1:p.Thr293Arg
NM_004960.3:c.890C>G , LRG_655t1:c.890C>G	NP_004951.1:p.Thr297Arg
NR_028388.2:n.960C>G
XM_005255233.3:c.275C>G	XP_005255290.1:p.Thr92Arg
XM_011545781.1:c.884C>G	XP_011544083.1:p.Thr295Arg
XM_011545782.1:c.275C>G	XP_011544084.1:p.Thr92Arg
XM_005255233.5:c.275C>G	XP_005255290.1:p.Thr92Arg
XM_011545782.2:c.275C>G	XP_011544084.1:p.Thr92Arg
XM_024450221.1:c.881C>G	XP_024305989.1:p.Thr294Arg
NM_004960.4:c.890C>G MANE Select	NP_004951.1:p.Thr297Arg