Canonical Allele Identifier: CA280594478

Gene: FUS

Linked Data

• dbSNP Id: rs1053950081
• MyVariant Identifiers: chr16:g.31196178T>A (hg19) ; chr16:g.31184857T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31184857T>A , CM000678.2:g.31184857T>A	GRCh38
NC_000016.9:g.31196178T>A , CM000678.1:g.31196178T>A	GRCh37
NC_000016.8:g.31103679T>A	NCBI36
NG_012889.2:g.9726T>A , LRG_655:g.9726T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.524-82T>A MANE Select	ENSP00000254108.8:n.524-82T>A
ENST00000254108.11:c.524-82T>A	ENSP00000254108.7:n.524-82T>A
ENST00000380244.7:c.521-82T>A	ENSP00000369594.3:n.521-82T>A
ENST00000487509.6:n.589-82T>A
ENST00000566605.5:c.524-82T>A	ENSP00000455073.1:n.524-82T>A
ENST00000568685.1:c.524-82T>A	ENSP00000455282.1:n.524-82T>A
NM_001170634.1:c.521-82T>A	NP_001164105.1:n.521-82T>A
NM_001170937.1:c.512-82T>A	NP_001164408.1:n.512-82T>A
NM_004960.3:c.524-82T>A , LRG_655t1:c.524-82T>A	NP_004951.1:n.524-82T>A
NR_028388.2:n.629-82T>A
XM_005255233.3:c.-57-82T>A	XP_005255290.1:n.-57-82T>A
XM_011545781.1:c.518-82T>A	XP_011544083.1:n.518-82T>A
XM_011545782.1:c.-57-82T>A	XP_011544084.1:n.-57-82T>A
XM_005255233.5:c.-57-82T>A	XP_005255290.1:n.-57-82T>A
XM_011545782.2:c.-57-82T>A	XP_011544084.1:n.-57-82T>A
XM_024450221.1:c.515-82T>A	XP_024305989.1:n.515-82T>A
NM_004960.4:c.524-82T>A MANE Select	NP_004951.1:n.524-82T>A