Canonical Allele Identifier: CA395677540

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31191430C>A , CM000678.2:g.31191430C>A	GRCh38
NC_000016.9:g.31202751C>A , CM000678.1:g.31202751C>A	GRCh37
NC_000016.8:g.31110252C>A	NCBI36
NG_012889.2:g.16299C>A , LRG_655:g.16299C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004960.4:c.1573C>A MANE Select	NP_004951.1:p.Pro525Thr
ENST00000254108.12:c.1573C>A MANE Select	ENSP00000254108.8:p.Pro525Thr
NM_001170634.1:c.1570C>A	NP_001164105.1:p.Pro524Thr
NM_001170937.1:c.1561C>A	NP_001164408.1:p.Pro521Thr
NM_004960.3:c.1573C>A , LRG_655t1:c.1573C>A	NP_004951.1:p.Pro525Thr
NR_028388.2:n.1643C>A
ENST00000254108.11:c.1573C>A	ENSP00000254108.7:p.Pro525Thr
ENST00000380244.7:c.1570C>A	ENSP00000369594.3:p.Pro524Thr
ENST00000483853.1:n.650C>A
ENST00000487509.6:n.4748C>A
ENST00000566605.5:c.*746C>A	ENSP00000455073.1:n.*746C>A
ENST00000568685.1:c.1576C>A	ENSP00000455282.1:p.Pro526Thr
ENST00000569760.5:n.464C>A
XM_005255233.3:c.958C>A	XP_005255290.1:p.Pro320Thr
XM_005255233.5:c.958C>A	XP_005255290.1:p.Pro320Thr
XM_011545781.1:c.1567C>A	XP_011544083.1:p.Pro523Thr
XM_011545782.1:c.958C>A	XP_011544084.1:p.Pro320Thr
XM_011545782.2:c.958C>A	XP_011544084.1:p.Pro320Thr
XM_024450221.1:c.1564C>A	XP_024305989.1:p.Pro522Thr