Canonical Allele Identifier: CA395672294

Gene: FUS

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.893T>G MANE Select	ENSP00000254108.8:p.Ile298Ser
ENST00000254108.11:c.893T>G	ENSP00000254108.7:p.Ile298Ser
ENST00000380244.7:c.890T>G	ENSP00000369594.3:p.Ile297Ser
ENST00000474990.5:n.187T>G
ENST00000487509.6:n.4068T>G
ENST00000564766.1:n.717T>G
ENST00000566605.5:c.*66T>G	ENSP00000455073.1:n.*66T>G
ENST00000568685.1:c.896T>G	ENSP00000455282.1:p.Ile299Ser
ENST00000568901.2:n.267T>G
NM_001170634.1:c.890T>G	NP_001164105.1:p.Ile297Ser
NM_001170937.1:c.881T>G	NP_001164408.1:p.Ile294Ser
NM_004960.3:c.893T>G , LRG_655t1:c.893T>G	NP_004951.1:p.Ile298Ser
NR_028388.2:n.963T>G
XM_005255233.3:c.278T>G	XP_005255290.1:p.Ile93Ser
XM_011545781.1:c.887T>G	XP_011544083.1:p.Ile296Ser
XM_011545782.1:c.278T>G	XP_011544084.1:p.Ile93Ser
XM_005255233.5:c.278T>G	XP_005255290.1:p.Ile93Ser
XM_011545782.2:c.278T>G	XP_011544084.1:p.Ile93Ser
XM_024450221.1:c.884T>G	XP_024305989.1:p.Ile295Ser
NM_004960.4:c.893T>G MANE Select	NP_004951.1:p.Ile298Ser