Canonical Allele Identifier: CA395669720

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31196322A>T (hg19) ; chr16:g.31185001A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31185001A>T , CM000678.2:g.31185001A>T	GRCh38
NC_000016.9:g.31196322A>T , CM000678.1:g.31196322A>T	GRCh37
NC_000016.8:g.31103823A>T	NCBI36
NG_012889.2:g.9870A>T , LRG_655:g.9870A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.586A>T MANE Select	ENSP00000254108.8:p.Asn196Tyr
ENST00000254108.11:c.586A>T	ENSP00000254108.7:p.Asn196Tyr
ENST00000380244.7:c.583A>T	ENSP00000369594.3:p.Asn195Tyr
ENST00000487509.6:n.651A>T
ENST00000566605.5:c.586A>T	ENSP00000455073.1:p.Asn196Tyr
ENST00000568685.1:c.586A>T	ENSP00000455282.1:p.Asn196Tyr
NM_001170634.1:c.583A>T	NP_001164105.1:p.Asn195Tyr
NM_001170937.1:c.574A>T	NP_001164408.1:p.Asn192Tyr
NM_004960.3:c.586A>T , LRG_655t1:c.586A>T	NP_004951.1:p.Asn196Tyr
NR_028388.2:n.691A>T
XM_005255233.3:c.6A>T	XP_005255290.1:p.Ala2=
XM_011545781.1:c.580A>T	XP_011544083.1:p.Asn194Tyr
XM_011545782.1:c.6A>T	XP_011544084.1:p.Ala2=
XM_005255233.5:c.6A>T	XP_005255290.1:p.Ala2=
XM_011545782.2:c.6A>T	XP_011544084.1:p.Ala2=
XM_024450221.1:c.577A>T	XP_024305989.1:p.Asn193Tyr
NM_004960.4:c.586A>T MANE Select	NP_004951.1:p.Asn196Tyr