Canonical Allele Identifier: CA395677534

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31191428G>T , CM000678.2:g.31191428G>T	GRCh38
NC_000016.9:g.31202749G>T , CM000678.1:g.31202749G>T	GRCh37
NC_000016.8:g.31110250G>T	NCBI36
NG_012889.2:g.16297G>T , LRG_655:g.16297G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004960.4:c.1571G>T MANE Select	NP_004951.1:p.Arg524Met
ENST00000254108.12:c.1571G>T MANE Select	ENSP00000254108.8:p.Arg524Met
NM_001170634.1:c.1568G>T	NP_001164105.1:p.Arg523Met
NM_001170937.1:c.1559G>T	NP_001164408.1:p.Arg520Met
NM_004960.3:c.1571G>T , LRG_655t1:c.1571G>T	NP_004951.1:p.Arg524Met
NR_028388.2:n.1641G>T
ENST00000254108.11:c.1571G>T	ENSP00000254108.7:p.Arg524Met
ENST00000380244.7:c.1568G>T	ENSP00000369594.3:p.Arg523Met
ENST00000483853.1:n.648G>T
ENST00000487509.6:n.4746G>T
ENST00000566605.5:c.*744G>T	ENSP00000455073.1:n.*744G>T
ENST00000568685.1:c.1574G>T	ENSP00000455282.1:p.Arg525Met
ENST00000569760.5:n.462G>T
XM_005255233.3:c.956G>T	XP_005255290.1:p.Arg319Met
XM_005255233.5:c.956G>T	XP_005255290.1:p.Arg319Met
XM_011545781.1:c.1565G>T	XP_011544083.1:p.Arg522Met
XM_011545782.1:c.956G>T	XP_011544084.1:p.Arg319Met
XM_011545782.2:c.956G>T	XP_011544084.1:p.Arg319Met
XM_024450221.1:c.1562G>T	XP_024305989.1:p.Arg521Met