Canonical Allele Identifier: CA395677576

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31191434A>G , CM000678.2:g.31191434A>G	GRCh38
NC_000016.9:g.31202755A>G , CM000678.1:g.31202755A>G	GRCh37
NC_000016.8:g.31110256A>G	NCBI36
NG_012889.2:g.16303A>G , LRG_655:g.16303A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004960.4:c.1577A>G MANE Select	NP_004951.1:p.Tyr526Cys
ENST00000254108.12:c.1577A>G MANE Select	ENSP00000254108.8:p.Tyr526Cys
NM_001170634.1:c.1574A>G	NP_001164105.1:p.Tyr525Cys
NM_001170937.1:c.1565A>G	NP_001164408.1:p.Tyr522Cys
NM_004960.3:c.1577A>G , LRG_655t1:c.1577A>G	NP_004951.1:p.Tyr526Cys
NR_028388.2:n.1647A>G
ENST00000254108.11:c.1577A>G	ENSP00000254108.7:p.Tyr526Cys
ENST00000380244.7:c.1574A>G	ENSP00000369594.3:p.Tyr525Cys
ENST00000483853.1:n.654A>G
ENST00000487509.6:n.4752A>G
ENST00000566605.5:c.*750A>G	ENSP00000455073.1:n.*750A>G
ENST00000568685.1:c.1580A>G	ENSP00000455282.1:p.Tyr527Cys
ENST00000569760.5:n.468A>G
XM_005255233.3:c.962A>G	XP_005255290.1:p.Tyr321Cys
XM_005255233.5:c.962A>G	XP_005255290.1:p.Tyr321Cys
XM_011545781.1:c.1571A>G	XP_011544083.1:p.Tyr524Cys
XM_011545782.1:c.962A>G	XP_011544084.1:p.Tyr321Cys
XM_011545782.2:c.962A>G	XP_011544084.1:p.Tyr321Cys
XM_024450221.1:c.1568A>G	XP_024305989.1:p.Tyr523Cys