Canonical Allele Identifier: CA2216944928

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31185175A= , CM000678.2:g.31185175A=	GRCh38
NC_000016.9:g.31196496A= , CM000678.1:g.31196496A=	GRCh37
NC_000016.8:g.31103997A=	NCBI36
NG_012889.2:g.10044A= , LRG_655:g.10044A=

Transcript Alleles

HGVS	Amino-acid Change
NM_004960.4:c.760A= MANE Select	NP_004951.1:p.Met254=
ENST00000254108.12:c.760A= MANE Select	ENSP00000254108.8:p.Met254=
NM_001170634.1:c.757A=	NP_001164105.1:p.Met253=
NM_001170937.1:c.748A=	NP_001164408.1:p.Met250=
NM_004960.3:c.760A= , LRG_655t1:c.760A=	NP_004951.1:p.Met254=
NR_028388.2:n.865A=
ENST00000254108.11:c.760A=	ENSP00000254108.7:p.Met254=
ENST00000380244.7:c.757A=	ENSP00000369594.3:p.Met253=
ENST00000487509.6:n.825A=
ENST00000566605.5:c.760A=	ENSP00000455073.1:p.Met254=
ENST00000568685.1:c.760A=	ENSP00000455282.1:p.Met254=
ENST00000570090.1:n.96A=
XM_005255233.3:c.180A=	XP_005255290.1:p.Ala60=
XM_005255233.5:c.180A=	XP_005255290.1:p.Ala60=
XM_011545781.1:c.754A=	XP_011544083.1:p.Met252=
XM_011545782.1:c.180A=	XP_011544084.1:p.Ala60=
XM_011545782.2:c.180A=	XP_011544084.1:p.Ala60=
XM_024450221.1:c.751A=	XP_024305989.1:p.Met251=