Canonical Allele Identifier: CA395669614

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31196290G>C (hg19) ; chr16:g.31184969G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31184969G>C , CM000678.2:g.31184969G>C	GRCh38
NC_000016.9:g.31196290G>C , CM000678.1:g.31196290G>C	GRCh37
NC_000016.8:g.31103791G>C	NCBI36
NG_012889.2:g.9838G>C , LRG_655:g.9838G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.554G>C MANE Select	ENSP00000254108.8:p.Ser185Thr
ENST00000254108.11:c.554G>C	ENSP00000254108.7:p.Ser185Thr
ENST00000380244.7:c.551G>C	ENSP00000369594.3:p.Ser184Thr
ENST00000487509.6:n.619G>C
ENST00000566605.5:c.554G>C	ENSP00000455073.1:p.Ser185Thr
ENST00000568685.1:c.554G>C	ENSP00000455282.1:p.Ser185Thr
NM_001170634.1:c.551G>C	NP_001164105.1:p.Ser184Thr
NM_001170937.1:c.542G>C	NP_001164408.1:p.Ser181Thr
NM_004960.3:c.554G>C , LRG_655t1:c.554G>C	NP_004951.1:p.Ser185Thr
NR_028388.2:n.659G>C
XM_005255233.3:c.-27G>C	XP_005255290.1:n.-27G>C
XM_011545781.1:c.548G>C	XP_011544083.1:p.Ser183Thr
XM_011545782.1:c.-27G>C	XP_011544084.1:n.-27G>C
XM_005255233.5:c.-27G>C	XP_005255290.1:n.-27G>C
XM_011545782.2:c.-27G>C	XP_011544084.1:n.-27G>C
XM_024450221.1:c.545G>C	XP_024305989.1:p.Ser182Thr
NM_004960.4:c.554G>C MANE Select	NP_004951.1:p.Ser185Thr