Canonical Allele Identifier: CA2216947172

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189182A= , CM000678.2:g.31189182A=	GRCh38
NC_000016.9:g.31200503A= , CM000678.1:g.31200503A=	GRCh37
NC_000016.8:g.31108004A=	NCBI36
NG_012889.2:g.14051A= , LRG_655:g.14051A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.892A= MANE Select	ENSP00000254108.8:p.Ile298=
ENST00000254108.11:c.892A=	ENSP00000254108.7:p.Ile298=
ENST00000380244.7:c.889A=	ENSP00000369594.3:p.Ile297=
ENST00000474990.5:n.186A=
ENST00000487509.6:n.4067A=
ENST00000564766.1:n.716A=
ENST00000566605.5:c.*65A=	ENSP00000455073.1:n.*65A=
ENST00000568685.1:c.895A=	ENSP00000455282.1:p.Ile299=
ENST00000568901.2:n.266A=
NM_001170634.1:c.889A=	NP_001164105.1:p.Ile297=
NM_001170937.1:c.880A=	NP_001164408.1:p.Ile294=
NM_004960.3:c.892A= , LRG_655t1:c.892A=	NP_004951.1:p.Ile298=
NR_028388.2:n.962A=
XM_005255233.3:c.277A=	XP_005255290.1:p.Ile93=
XM_011545781.1:c.886A=	XP_011544083.1:p.Ile296=
XM_011545782.1:c.277A=	XP_011544084.1:p.Ile93=
XM_005255233.5:c.277A=	XP_005255290.1:p.Ile93=
XM_011545782.2:c.277A=	XP_011544084.1:p.Ile93=
XM_024450221.1:c.883A=	XP_024305989.1:p.Ile295=
NM_004960.4:c.892A= MANE Select	NP_004951.1:p.Ile298=