Canonical Allele Identifier: CA395669609

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31196289A>C (hg19) ; chr16:g.31184968A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31184968A>C , CM000678.2:g.31184968A>C	GRCh38
NC_000016.9:g.31196289A>C , CM000678.1:g.31196289A>C	GRCh37
NC_000016.8:g.31103790A>C	NCBI36
NG_012889.2:g.9837A>C , LRG_655:g.9837A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.553A>C MANE Select	ENSP00000254108.8:p.Ser185Arg
ENST00000254108.11:c.553A>C	ENSP00000254108.7:p.Ser185Arg
ENST00000380244.7:c.550A>C	ENSP00000369594.3:p.Ser184Arg
ENST00000487509.6:n.618A>C
ENST00000566605.5:c.553A>C	ENSP00000455073.1:p.Ser185Arg
ENST00000568685.1:c.553A>C	ENSP00000455282.1:p.Ser185Arg
NM_001170634.1:c.550A>C	NP_001164105.1:p.Ser184Arg
NM_001170937.1:c.541A>C	NP_001164408.1:p.Ser181Arg
NM_004960.3:c.553A>C , LRG_655t1:c.553A>C	NP_004951.1:p.Ser185Arg
NR_028388.2:n.658A>C
XM_005255233.3:c.-28A>C	XP_005255290.1:n.-28A>C
XM_011545781.1:c.547A>C	XP_011544083.1:p.Ser183Arg
XM_011545782.1:c.-28A>C	XP_011544084.1:n.-28A>C
XM_005255233.5:c.-28A>C	XP_005255290.1:n.-28A>C
XM_011545782.2:c.-28A>C	XP_011544084.1:n.-28A>C
XM_024450221.1:c.544A>C	XP_024305989.1:p.Ser182Arg
NM_004960.4:c.553A>C MANE Select	NP_004951.1:p.Ser185Arg