Canonical Allele Identifier: CA2216944615

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31184944T= , CM000678.2:g.31184944T=	GRCh38
NC_000016.9:g.31196265T= , CM000678.1:g.31196265T=	GRCh37
NC_000016.8:g.31103766T=	NCBI36
NG_012889.2:g.9813T= , LRG_655:g.9813T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.529T= MANE Select	ENSP00000254108.8:p.Tyr177=
ENST00000254108.11:c.529T=	ENSP00000254108.7:p.Tyr177=
ENST00000380244.7:c.526T=	ENSP00000369594.3:p.Tyr176=
ENST00000487509.6:n.594T=
ENST00000566605.5:c.529T=	ENSP00000455073.1:p.Tyr177=
ENST00000568685.1:c.529T=	ENSP00000455282.1:p.Tyr177=
NM_001170634.1:c.526T=	NP_001164105.1:p.Tyr176=
NM_001170937.1:c.517T=	NP_001164408.1:p.Tyr173=
NM_004960.3:c.529T= , LRG_655t1:c.529T=	NP_004951.1:p.Tyr177=
NR_028388.2:n.634T=
XM_005255233.3:c.-52T=	XP_005255290.1:n.-52T=
XM_011545781.1:c.523T=	XP_011544083.1:p.Tyr175=
XM_011545782.1:c.-52T=	XP_011544084.1:n.-52T=
XM_005255233.5:c.-52T=	XP_005255290.1:n.-52T=
XM_011545782.2:c.-52T=	XP_011544084.1:n.-52T=
XM_024450221.1:c.520T=	XP_024305989.1:p.Tyr174=
NM_004960.4:c.529T= MANE Select	NP_004951.1:p.Tyr177=