Canonical Allele Identifier: CA8023630

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31184357A>C , CM000678.2:g.31184357A>C	GRCh38
NC_000016.9:g.31195678A>C , CM000678.1:g.31195678A>C	GRCh37
NC_000016.8:g.31103179A>C	NCBI36
NG_012889.2:g.9226A>C , LRG_655:g.9226A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_004960.4:c.484A>C MANE Select	NP_004951.1:p.Asn162His
ENST00000254108.12:c.484A>C MANE Select	ENSP00000254108.8:p.Asn162His
NM_001170634.1:c.481A>C	NP_001164105.1:p.Asn161His
NM_001170937.1:c.484A>C	NP_001164408.1:p.Asn162His
NM_004960.3:c.484A>C , LRG_655t1:c.484A>C	NP_004951.1:p.Asn162His
NR_028388.2:n.589A>C
ENST00000254108.11:c.484A>C	ENSP00000254108.7:p.Asn162His
ENST00000380244.7:c.481A>C	ENSP00000369594.3:p.Asn161His
ENST00000487509.6:n.549A>C
ENST00000487974.1:n.602A>C
ENST00000566605.5:c.484A>C	ENSP00000455073.1:p.Asn162His
ENST00000568685.1:c.484A>C	ENSP00000455282.1:p.Asn162His
XM_005255233.3:c.-97A>C	XP_005255290.1:n.-97A>C
XM_005255233.5:c.-97A>C	XP_005255290.1:n.-97A>C
XM_011545781.1:c.484A>C	XP_011544083.1:p.Asn162His
XM_011545782.1:c.-91A>C	XP_011544084.1:n.-91A>C
XM_024450221.1:c.481A>C	XP_024305989.1:p.Asn161His