Canonical Allele Identifier: CA395677434

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31202738T>G (hg19) ; chr16:g.31191417T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31191417T>G , CM000678.2:g.31191417T>G	GRCh38
NC_000016.9:g.31202738T>G , CM000678.1:g.31202738T>G	GRCh37
NC_000016.8:g.31110239T>G	NCBI36
NG_012889.2:g.16286T>G , LRG_655:g.16286T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000254108.12:c.1560T>G MANE Select	ENSP00000254108.8:p.Asp520Glu
ENST00000254108.11:c.1560T>G	ENSP00000254108.7:p.Asp520Glu
ENST00000380244.7:c.1557T>G	ENSP00000369594.3:p.Asp519Glu
ENST00000483853.1:n.637T>G
ENST00000487509.6:n.4735T>G
ENST00000566605.5:c.*733T>G	ENSP00000455073.1:n.*733T>G
ENST00000568685.1:c.1563T>G	ENSP00000455282.1:p.Asp521Glu
ENST00000569760.5:n.451T>G
NM_001170634.1:c.1557T>G	NP_001164105.1:p.Asp519Glu
NM_001170937.1:c.1548T>G	NP_001164408.1:p.Asp516Glu
NM_004960.3:c.1560T>G , LRG_655t1:c.1560T>G	NP_004951.1:p.Asp520Glu
NR_028388.2:n.1630T>G
XM_005255233.3:c.945T>G	XP_005255290.1:p.Asp315Glu
XM_011545781.1:c.1554T>G	XP_011544083.1:p.Asp518Glu
XM_011545782.1:c.945T>G	XP_011544084.1:p.Asp315Glu
XM_005255233.5:c.945T>G	XP_005255290.1:p.Asp315Glu
XM_011545782.2:c.945T>G	XP_011544084.1:p.Asp315Glu
XM_024450221.1:c.1551T>G	XP_024305989.1:p.Asp517Glu
NM_004960.4:c.1560T>G MANE Select	NP_004951.1:p.Asp520Glu