Canonical Allele Identifier: CA395672319

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31200509T>A (hg19) ; chr16:g.31189188T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189188T>A , CM000678.2:g.31189188T>A	GRCh38
NC_000016.9:g.31200509T>A , CM000678.1:g.31200509T>A	GRCh37
NC_000016.8:g.31108010T>A	NCBI36
NG_012889.2:g.14057T>A , LRG_655:g.14057T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.898T>A MANE Select	ENSP00000254108.8:p.Ser300Thr
ENST00000254108.11:c.898T>A	ENSP00000254108.7:p.Ser300Thr
ENST00000380244.7:c.895T>A	ENSP00000369594.3:p.Ser299Thr
ENST00000474990.5:n.192T>A
ENST00000487509.6:n.4073T>A
ENST00000564766.1:n.722T>A
ENST00000566605.5:c.*71T>A	ENSP00000455073.1:n.*71T>A
ENST00000568685.1:c.901T>A	ENSP00000455282.1:p.Ser301Thr
ENST00000568901.2:n.272T>A
NM_001170634.1:c.895T>A	NP_001164105.1:p.Ser299Thr
NM_001170937.1:c.886T>A	NP_001164408.1:p.Ser296Thr
NM_004960.3:c.898T>A , LRG_655t1:c.898T>A	NP_004951.1:p.Ser300Thr
NR_028388.2:n.968T>A
XM_005255233.3:c.283T>A	XP_005255290.1:p.Ser95Thr
XM_011545781.1:c.892T>A	XP_011544083.1:p.Ser298Thr
XM_011545782.1:c.283T>A	XP_011544084.1:p.Ser95Thr
XM_005255233.5:c.283T>A	XP_005255290.1:p.Ser95Thr
XM_011545782.2:c.283T>A	XP_011544084.1:p.Ser95Thr
XM_024450221.1:c.889T>A	XP_024305989.1:p.Ser297Thr
NM_004960.4:c.898T>A MANE Select	NP_004951.1:p.Ser300Thr