Canonical Allele Identifier: CA395677401

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31202734A>T (hg19) ; chr16:g.31191413A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31191413A>T , CM000678.2:g.31191413A>T	GRCh38
NC_000016.9:g.31202734A>T , CM000678.1:g.31202734A>T	GRCh37
NC_000016.8:g.31110235A>T	NCBI36
NG_012889.2:g.16282A>T , LRG_655:g.16282A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000254108.12:c.1556A>T MANE Select	ENSP00000254108.8:p.Gln519Leu
ENST00000254108.11:c.1556A>T	ENSP00000254108.7:p.Gln519Leu
ENST00000380244.7:c.1553A>T	ENSP00000369594.3:p.Gln518Leu
ENST00000483853.1:n.633A>T
ENST00000487509.6:n.4731A>T
ENST00000566605.5:c.*729A>T	ENSP00000455073.1:n.*729A>T
ENST00000568685.1:c.1559A>T	ENSP00000455282.1:p.Gln520Leu
ENST00000569760.5:n.447A>T
NM_001170634.1:c.1553A>T	NP_001164105.1:p.Gln518Leu
NM_001170937.1:c.1544A>T	NP_001164408.1:p.Gln515Leu
NM_004960.3:c.1556A>T , LRG_655t1:c.1556A>T	NP_004951.1:p.Gln519Leu
NR_028388.2:n.1626A>T
XM_005255233.3:c.941A>T	XP_005255290.1:p.Gln314Leu
XM_011545781.1:c.1550A>T	XP_011544083.1:p.Gln517Leu
XM_011545782.1:c.941A>T	XP_011544084.1:p.Gln314Leu
XM_005255233.5:c.941A>T	XP_005255290.1:p.Gln314Leu
XM_011545782.2:c.941A>T	XP_011544084.1:p.Gln314Leu
XM_024450221.1:c.1547A>T	XP_024305989.1:p.Gln516Leu
NM_004960.4:c.1556A>T MANE Select	NP_004951.1:p.Gln519Leu