Canonical Allele Identifier: CA395672296

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31200504T>A (hg19) ; chr16:g.31189183T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189183T>A , CM000678.2:g.31189183T>A	GRCh38
NC_000016.9:g.31200504T>A , CM000678.1:g.31200504T>A	GRCh37
NC_000016.8:g.31108005T>A	NCBI36
NG_012889.2:g.14052T>A , LRG_655:g.14052T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.893T>A MANE Select	ENSP00000254108.8:p.Ile298Asn
ENST00000254108.11:c.893T>A	ENSP00000254108.7:p.Ile298Asn
ENST00000380244.7:c.890T>A	ENSP00000369594.3:p.Ile297Asn
ENST00000474990.5:n.187T>A
ENST00000487509.6:n.4068T>A
ENST00000564766.1:n.717T>A
ENST00000566605.5:c.*66T>A	ENSP00000455073.1:n.*66T>A
ENST00000568685.1:c.896T>A	ENSP00000455282.1:p.Ile299Asn
ENST00000568901.2:n.267T>A
NM_001170634.1:c.890T>A	NP_001164105.1:p.Ile297Asn
NM_001170937.1:c.881T>A	NP_001164408.1:p.Ile294Asn
NM_004960.3:c.893T>A , LRG_655t1:c.893T>A	NP_004951.1:p.Ile298Asn
NR_028388.2:n.963T>A
XM_005255233.3:c.278T>A	XP_005255290.1:p.Ile93Asn
XM_011545781.1:c.887T>A	XP_011544083.1:p.Ile296Asn
XM_011545782.1:c.278T>A	XP_011544084.1:p.Ile93Asn
XM_005255233.5:c.278T>A	XP_005255290.1:p.Ile93Asn
XM_011545782.2:c.278T>A	XP_011544084.1:p.Ile93Asn
XM_024450221.1:c.884T>A	XP_024305989.1:p.Ile295Asn
NM_004960.4:c.893T>A MANE Select	NP_004951.1:p.Ile298Asn