Canonical Allele Identifier: CA2216944268

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31184901T= , CM000678.2:g.31184901T=	GRCh38
NC_000016.9:g.31196222T= , CM000678.1:g.31196222T=	GRCh37
NC_000016.8:g.31103723T=	NCBI36
NG_012889.2:g.9770T= , LRG_655:g.9770T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.524-38T= MANE Select	ENSP00000254108.8:n.524-38T=
ENST00000254108.11:c.524-38T=	ENSP00000254108.7:n.524-38T=
ENST00000380244.7:c.521-38T=	ENSP00000369594.3:n.521-38T=
ENST00000487509.6:n.589-38T=
ENST00000566605.5:c.524-38T=	ENSP00000455073.1:n.524-38T=
ENST00000568685.1:c.524-38T=	ENSP00000455282.1:n.524-38T=
NM_001170634.1:c.521-38T=	NP_001164105.1:n.521-38T=
NM_001170937.1:c.512-38T=	NP_001164408.1:n.512-38T=
NM_004960.3:c.524-38T= , LRG_655t1:c.524-38T=	NP_004951.1:n.524-38T=
NR_028388.2:n.629-38T=
XM_005255233.3:c.-57-38T=	XP_005255290.1:n.-57-38T=
XM_011545781.1:c.518-38T=	XP_011544083.1:n.518-38T=
XM_011545782.1:c.-57-38T=	XP_011544084.1:n.-57-38T=
XM_005255233.5:c.-57-38T=	XP_005255290.1:n.-57-38T=
XM_011545782.2:c.-57-38T=	XP_011544084.1:n.-57-38T=
XM_024450221.1:c.515-38T=	XP_024305989.1:n.515-38T=
NM_004960.4:c.524-38T= MANE Select	NP_004951.1:n.524-38T=