Canonical Allele Identifier: CA395672397

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31200520T>G (hg19) ; chr16:g.31189199T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189199T>G , CM000678.2:g.31189199T>G	GRCh38
NC_000016.9:g.31200520T>G , CM000678.1:g.31200520T>G	GRCh37
NC_000016.8:g.31108021T>G	NCBI36
NG_012889.2:g.14068T>G , LRG_655:g.14068T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.909T>G MANE Select	ENSP00000254108.8:p.Asp303Glu
ENST00000254108.11:c.909T>G	ENSP00000254108.7:p.Asp303Glu
ENST00000380244.7:c.906T>G	ENSP00000369594.3:p.Asp302Glu
ENST00000474990.5:n.203T>G
ENST00000487509.6:n.4084T>G
ENST00000564766.1:n.733T>G
ENST00000566605.5:c.*82T>G	ENSP00000455073.1:n.*82T>G
ENST00000568685.1:c.912T>G	ENSP00000455282.1:p.Asp304Glu
ENST00000568901.2:n.283T>G
NM_001170634.1:c.906T>G	NP_001164105.1:p.Asp302Glu
NM_001170937.1:c.897T>G	NP_001164408.1:p.Asp299Glu
NM_004960.3:c.909T>G , LRG_655t1:c.909T>G	NP_004951.1:p.Asp303Glu
NR_028388.2:n.979T>G
XM_005255233.3:c.294T>G	XP_005255290.1:p.Asp98Glu
XM_011545781.1:c.903T>G	XP_011544083.1:p.Asp301Glu
XM_011545782.1:c.294T>G	XP_011544084.1:p.Asp98Glu
XM_005255233.5:c.294T>G	XP_005255290.1:p.Asp98Glu
XM_011545782.2:c.294T>G	XP_011544084.1:p.Asp98Glu
XM_024450221.1:c.900T>G	XP_024305989.1:p.Asp300Glu
NM_004960.4:c.909T>G MANE Select	NP_004951.1:p.Asp303Glu