Canonical Allele Identifier: CA2216907348

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31191481A= , CM000678.2:g.31191481A=	GRCh38
NC_000016.9:g.31202802A= , CM000678.1:g.31202802A=	GRCh37
NC_000016.8:g.31110303A=	NCBI36
NG_012889.2:g.16350A= , LRG_655:g.16350A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.*43A= MANE Select	ENSP00000254108.8:n.*43A=
ENST00000254108.11:c.*43A=	ENSP00000254108.7:n.*43A=
ENST00000380244.7:c.*43A=	ENSP00000369594.3:n.*43A=
ENST00000483853.1:n.701A=
ENST00000487509.6:n.4799A=
ENST00000566605.5:c.*797A=	ENSP00000455073.1:n.*797A=
ENST00000568685.1:c.*43A=	ENSP00000455282.1:n.*43A=
ENST00000569760.5:n.515A=
NM_001170634.1:c.*43A=	NP_001164105.1:n.*43A=
NM_001170937.1:c.*43A=	NP_001164408.1:n.*43A=
NM_004960.3:c.*43A= , LRG_655t1:c.*43A=	NP_004951.1:n.*43A=
NR_028388.2:n.1694A=
XM_005255233.3:c.*43A=	XP_005255290.1:n.*43A=
XM_011545781.1:c.*43A=	XP_011544083.1:n.*43A=
XM_011545782.1:c.*43A=	XP_011544084.1:n.*43A=
XM_005255233.5:c.*43A=	XP_005255290.1:n.*43A=
XM_011545782.2:c.*43A=	XP_011544084.1:n.*43A=
XM_024450221.1:c.*43A=	XP_024305989.1:n.*43A=
NM_004960.4:c.*43A= MANE Select	NP_004951.1:n.*43A=