Canonical Allele Identifier: CA2216942119

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31183870C= , CM000678.2:g.31183870C=	GRCh38
NC_000016.9:g.31195191C= , CM000678.1:g.31195191C=	GRCh37
NC_000016.8:g.31102692C=	NCBI36
NG_012889.2:g.8739C= , LRG_655:g.8739C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.203C= MANE Select	ENSP00000254108.8:p.Thr68=
ENST00000254108.11:c.203C=	ENSP00000254108.7:p.Thr68=
ENST00000380244.7:c.200C=	ENSP00000369594.3:p.Thr67=
ENST00000487509.6:n.268C=
ENST00000487974.1:n.321C=
ENST00000566605.5:c.203C=	ENSP00000455073.1:p.Thr68=
ENST00000568685.1:c.203C=	ENSP00000455282.1:p.Thr68=
NM_001170634.1:c.200C=	NP_001164105.1:p.Thr67=
NM_001170937.1:c.203C=	NP_001164408.1:p.Thr68=
NM_004960.3:c.203C= , LRG_655t1:c.203C=	NP_004951.1:p.Thr68=
NR_028388.2:n.308C=
XM_005255233.3:c.-378C=	XP_005255290.1:n.-378C=
XM_011545781.1:c.203C=	XP_011544083.1:p.Thr68=
XM_005255233.5:c.-378C=	XP_005255290.1:n.-378C=
XM_024450221.1:c.200C=	XP_024305989.1:p.Thr67=
NM_004960.4:c.203C= MANE Select	NP_004951.1:p.Thr68=