Canonical Allele Identifier: CA2216944264

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31184900T= , CM000678.2:g.31184900T=	GRCh38
NC_000016.9:g.31196221T= , CM000678.1:g.31196221T=	GRCh37
NC_000016.8:g.31103722T=	NCBI36
NG_012889.2:g.9769T= , LRG_655:g.9769T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.524-39T= MANE Select	ENSP00000254108.8:n.524-39T=
ENST00000254108.11:c.524-39T=	ENSP00000254108.7:n.524-39T=
ENST00000380244.7:c.521-39T=	ENSP00000369594.3:n.521-39T=
ENST00000487509.6:n.589-39T=
ENST00000566605.5:c.524-39T=	ENSP00000455073.1:n.524-39T=
ENST00000568685.1:c.524-39T=	ENSP00000455282.1:n.524-39T=
NM_001170634.1:c.521-39T=	NP_001164105.1:n.521-39T=
NM_001170937.1:c.512-39T=	NP_001164408.1:n.512-39T=
NM_004960.3:c.524-39T= , LRG_655t1:c.524-39T=	NP_004951.1:n.524-39T=
NR_028388.2:n.629-39T=
XM_005255233.3:c.-57-39T=	XP_005255290.1:n.-57-39T=
XM_011545781.1:c.518-39T=	XP_011544083.1:n.518-39T=
XM_011545782.1:c.-57-39T=	XP_011544084.1:n.-57-39T=
XM_005255233.5:c.-57-39T=	XP_005255290.1:n.-57-39T=
XM_011545782.2:c.-57-39T=	XP_011544084.1:n.-57-39T=
XM_024450221.1:c.515-39T=	XP_024305989.1:n.515-39T=
NM_004960.4:c.524-39T= MANE Select	NP_004951.1:n.524-39T=