Canonical Allele Identifier: CA2216944847

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31185061C= , CM000678.2:g.31185061C=	GRCh38
NC_000016.9:g.31196382C= , CM000678.1:g.31196382C=	GRCh37
NC_000016.8:g.31103883C=	NCBI36
NG_012889.2:g.9930C= , LRG_655:g.9930C=

Transcript Alleles

HGVS	Amino-acid Change
NM_004960.4:c.646C= MANE Select	NP_004951.1:p.Arg216=
ENST00000254108.12:c.646C= MANE Select	ENSP00000254108.8:p.Arg216=
NM_001170634.1:c.643C=	NP_001164105.1:p.Arg215=
NM_001170937.1:c.634C=	NP_001164408.1:p.Arg212=
NM_004960.3:c.646C= , LRG_655t1:c.646C=	NP_004951.1:p.Arg216=
NR_028388.2:n.751C=
ENST00000254108.11:c.646C=	ENSP00000254108.7:p.Arg216=
ENST00000380244.7:c.643C=	ENSP00000369594.3:p.Arg215=
ENST00000487509.6:n.711C=
ENST00000566605.5:c.646C=	ENSP00000455073.1:p.Arg216=
ENST00000568685.1:c.646C=	ENSP00000455282.1:p.Arg216=
XM_005255233.3:c.66C=	XP_005255290.1:p.Ala22=
XM_005255233.5:c.66C=	XP_005255290.1:p.Ala22=
XM_011545781.1:c.640C=	XP_011544083.1:p.Arg214=
XM_011545782.1:c.66C=	XP_011544084.1:p.Ala22=
XM_011545782.2:c.66C=	XP_011544084.1:p.Ala22=
XM_024450221.1:c.637C=	XP_024305989.1:p.Arg213=