Canonical Allele Identifier: CA395669727

Gene: FUS

Linked Data

• dbSNP Id: rs755591829
• gnomAD v3: 16-31185002-A-C
• gnomAD v4: 16-31185002-A-C
• MyVariant Identifiers: chr16:g.31196323A>C (hg19) ; chr16:g.31185002A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31185002A>C , CM000678.2:g.31185002A>C	GRCh38
NC_000016.9:g.31196323A>C , CM000678.1:g.31196323A>C	GRCh37
NC_000016.8:g.31103824A>C	NCBI36
NG_012889.2:g.9871A>C , LRG_655:g.9871A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.587A>C MANE Select	ENSP00000254108.8:p.Asn196Thr
ENST00000254108.11:c.587A>C	ENSP00000254108.7:p.Asn196Thr
ENST00000380244.7:c.584A>C	ENSP00000369594.3:p.Asn195Thr
ENST00000487509.6:n.652A>C
ENST00000566605.5:c.587A>C	ENSP00000455073.1:p.Asn196Thr
ENST00000568685.1:c.587A>C	ENSP00000455282.1:p.Asn196Thr
NM_001170634.1:c.584A>C	NP_001164105.1:p.Asn195Thr
NM_001170937.1:c.575A>C	NP_001164408.1:p.Asn192Thr
NM_004960.3:c.587A>C , LRG_655t1:c.587A>C	NP_004951.1:p.Asn196Thr
NR_028388.2:n.692A>C
XM_005255233.3:c.7A>C	XP_005255290.1:p.Ile3Leu
XM_011545781.1:c.581A>C	XP_011544083.1:p.Asn194Thr
XM_011545782.1:c.7A>C	XP_011544084.1:p.Ile3Leu
XM_005255233.5:c.7A>C	XP_005255290.1:p.Ile3Leu
XM_011545782.2:c.7A>C	XP_011544084.1:p.Ile3Leu
XM_024450221.1:c.578A>C	XP_024305989.1:p.Asn193Thr
NM_004960.4:c.587A>C MANE Select	NP_004951.1:p.Asn196Thr