Canonical Allele Identifier: CA395672370

Gene: FUS

Linked Data

• dbSNP Id: rs2079315566
• MyVariant Identifiers: chr16:g.31200516C>T (hg19) ; chr16:g.31189195C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189195C>T , CM000678.2:g.31189195C>T	GRCh38
NC_000016.9:g.31200516C>T , CM000678.1:g.31200516C>T	GRCh37
NC_000016.8:g.31108017C>T	NCBI36
NG_012889.2:g.14064C>T , LRG_655:g.14064C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.905C>T MANE Select	ENSP00000254108.8:p.Ala302Val
ENST00000254108.11:c.905C>T	ENSP00000254108.7:p.Ala302Val
ENST00000380244.7:c.902C>T	ENSP00000369594.3:p.Ala301Val
ENST00000474990.5:n.199C>T
ENST00000487509.6:n.4080C>T
ENST00000564766.1:n.729C>T
ENST00000566605.5:c.*78C>T	ENSP00000455073.1:n.*78C>T
ENST00000568685.1:c.908C>T	ENSP00000455282.1:p.Ala303Val
ENST00000568901.2:n.279C>T
NM_001170634.1:c.902C>T	NP_001164105.1:p.Ala301Val
NM_001170937.1:c.893C>T	NP_001164408.1:p.Ala298Val
NM_004960.3:c.905C>T , LRG_655t1:c.905C>T	NP_004951.1:p.Ala302Val
NR_028388.2:n.975C>T
XM_005255233.3:c.290C>T	XP_005255290.1:p.Ala97Val
XM_011545781.1:c.899C>T	XP_011544083.1:p.Ala300Val
XM_011545782.1:c.290C>T	XP_011544084.1:p.Ala97Val
XM_005255233.5:c.290C>T	XP_005255290.1:p.Ala97Val
XM_011545782.2:c.290C>T	XP_011544084.1:p.Ala97Val
XM_024450221.1:c.896C>T	XP_024305989.1:p.Ala299Val
NM_004960.4:c.905C>T MANE Select	NP_004951.1:p.Ala302Val