Canonical Allele Identifier: CA2632833803

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31182155A>C , CM000678.2:g.31182155A>C	GRCh38
NC_000016.9:g.31193476A>C , CM000678.1:g.31193476A>C	GRCh37
NC_000016.8:g.31100977A>C	NCBI36
NG_012889.2:g.7024A>C , LRG_655:g.7024A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_004960.4:c.14-243A>C MANE Select	NP_004951.1:n.14-243A>C
ENST00000254108.12:c.14-243A>C MANE Select	ENSP00000254108.8:n.14-243A>C
NM_001170634.1:c.14-243A>C	NP_001164105.1:n.14-243A>C
NM_001170937.1:c.14-243A>C	NP_001164408.1:n.14-243A>C
NM_004960.3:c.14-243A>C , LRG_655t1:c.14-243A>C	NP_004951.1:n.14-243A>C
NR_028388.2:n.119-243A>C
ENST00000254108.11:c.14-243A>C	ENSP00000254108.7:n.14-243A>C
ENST00000380244.7:c.14-243A>C	ENSP00000369594.3:n.14-243A>C
ENST00000487045.6:n.90-243A>C
ENST00000487509.6:n.79-243A>C
ENST00000566605.5:c.14-243A>C	ENSP00000455073.1:n.14-243A>C
ENST00000568685.1:c.14-243A>C	ENSP00000455282.1:n.14-243A>C
XM_005255233.3:c.-564-243A>C	XP_005255290.1:n.-564-243A>C
XM_005255233.5:c.-564-243A>C	XP_005255290.1:n.-564-243A>C
XM_011545781.1:c.14-243A>C	XP_011544083.1:n.14-243A>C
XM_024450221.1:c.14-243A>C	XP_024305989.1:n.14-243A>C