Canonical Allele Identifier: CA395677370

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31202731G>T (hg19) ; chr16:g.31191410G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31191410G>T , CM000678.2:g.31191410G>T	GRCh38
NC_000016.9:g.31202731G>T , CM000678.1:g.31202731G>T	GRCh37
NC_000016.8:g.31110232G>T	NCBI36
NG_012889.2:g.16279G>T , LRG_655:g.16279G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000254108.12:c.1553G>T MANE Select	ENSP00000254108.8:p.Arg518Ile
ENST00000254108.11:c.1553G>T	ENSP00000254108.7:p.Arg518Ile
ENST00000380244.7:c.1550G>T	ENSP00000369594.3:p.Arg517Ile
ENST00000483853.1:n.630G>T
ENST00000487509.6:n.4728G>T
ENST00000566605.5:c.*726G>T	ENSP00000455073.1:n.*726G>T
ENST00000568685.1:c.1556G>T	ENSP00000455282.1:p.Arg519Ile
ENST00000569760.5:n.444G>T
NM_001170634.1:c.1550G>T	NP_001164105.1:p.Arg517Ile
NM_001170937.1:c.1541G>T	NP_001164408.1:p.Arg514Ile
NM_004960.3:c.1553G>T , LRG_655t1:c.1553G>T	NP_004951.1:p.Arg518Ile
NR_028388.2:n.1623G>T
XM_005255233.3:c.938G>T	XP_005255290.1:p.Arg313Ile
XM_011545781.1:c.1547G>T	XP_011544083.1:p.Arg516Ile
XM_011545782.1:c.938G>T	XP_011544084.1:p.Arg313Ile
XM_005255233.5:c.938G>T	XP_005255290.1:p.Arg313Ile
XM_011545782.2:c.938G>T	XP_011544084.1:p.Arg313Ile
XM_024450221.1:c.1544G>T	XP_024305989.1:p.Arg515Ile
NM_004960.4:c.1553G>T MANE Select	NP_004951.1:p.Arg518Ile