Canonical Allele Identifier: CA395672273

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31200500A>T (hg19) ; chr16:g.31189179A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189179A>T , CM000678.2:g.31189179A>T	GRCh38
NC_000016.9:g.31200500A>T , CM000678.1:g.31200500A>T	GRCh37
NC_000016.8:g.31108001A>T	NCBI36
NG_012889.2:g.14048A>T , LRG_655:g.14048A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.889A>T MANE Select	ENSP00000254108.8:p.Thr297Ser
ENST00000254108.11:c.889A>T	ENSP00000254108.7:p.Thr297Ser
ENST00000380244.7:c.886A>T	ENSP00000369594.3:p.Thr296Ser
ENST00000474990.5:n.183A>T
ENST00000487509.6:n.4064A>T
ENST00000564766.1:n.713A>T
ENST00000566605.5:c.*62A>T	ENSP00000455073.1:n.*62A>T
ENST00000568685.1:c.892A>T	ENSP00000455282.1:p.Thr298Ser
ENST00000568901.2:n.263A>T
NM_001170634.1:c.886A>T	NP_001164105.1:p.Thr296Ser
NM_001170937.1:c.877A>T	NP_001164408.1:p.Thr293Ser
NM_004960.3:c.889A>T , LRG_655t1:c.889A>T	NP_004951.1:p.Thr297Ser
NR_028388.2:n.959A>T
XM_005255233.3:c.274A>T	XP_005255290.1:p.Thr92Ser
XM_011545781.1:c.883A>T	XP_011544083.1:p.Thr295Ser
XM_011545782.1:c.274A>T	XP_011544084.1:p.Thr92Ser
XM_005255233.5:c.274A>T	XP_005255290.1:p.Thr92Ser
XM_011545782.2:c.274A>T	XP_011544084.1:p.Thr92Ser
XM_024450221.1:c.880A>T	XP_024305989.1:p.Thr294Ser
NM_004960.4:c.889A>T MANE Select	NP_004951.1:p.Thr297Ser