Canonical Allele Identifier: CA8023715

Gene: FUS

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
NM_004960.4:c.587A>G MANE Select	NP_004951.1:p.Asn196Ser
ENST00000254108.12:c.587A>G MANE Select	ENSP00000254108.8:p.Asn196Ser
NM_001170634.1:c.584A>G	NP_001164105.1:p.Asn195Ser
NM_001170937.1:c.575A>G	NP_001164408.1:p.Asn192Ser
NM_004960.3:c.587A>G , LRG_655t1:c.587A>G	NP_004951.1:p.Asn196Ser
NR_028388.2:n.692A>G
ENST00000254108.11:c.587A>G	ENSP00000254108.7:p.Asn196Ser
ENST00000380244.7:c.584A>G	ENSP00000369594.3:p.Asn195Ser
ENST00000487509.6:n.652A>G
ENST00000566605.5:c.587A>G	ENSP00000455073.1:p.Asn196Ser
ENST00000568685.1:c.587A>G	ENSP00000455282.1:p.Asn196Ser
XM_005255233.3:c.7A>G	XP_005255290.1:p.Ile3Val
XM_005255233.5:c.7A>G	XP_005255290.1:p.Ile3Val
XM_011545781.1:c.581A>G	XP_011544083.1:p.Asn194Ser
XM_011545782.1:c.7A>G	XP_011544084.1:p.Ile3Val
XM_011545782.2:c.7A>G	XP_011544084.1:p.Ile3Val
XM_024450221.1:c.578A>G	XP_024305989.1:p.Asn193Ser