Canonical Allele Identifier: CA494715365

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31202741C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31191420C>G , CM000678.2:g.31191420C>G	GRCh38
NC_000016.9:g.31202741C>G , CM000678.1:g.31202741C>G	GRCh37
NC_000016.8:g.31110242C>G	NCBI36
NG_012889.2:g.16289C>G , LRG_655:g.16289C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000254108.12:c.1563C>G MANE Select	ENSP00000254108.8:p.Arg521=
ENST00000254108.11:c.1563C>G	ENSP00000254108.7:p.Arg521=
ENST00000380244.7:c.1560C>G	ENSP00000369594.3:p.Arg520=
ENST00000483853.1:n.640C>G
ENST00000487509.6:n.4738C>G
ENST00000566605.5:c.*736C>G	ENSP00000455073.1:n.*736C>G
ENST00000568685.1:c.1566C>G	ENSP00000455282.1:p.Arg522=
ENST00000569760.5:n.454C>G
NM_001170634.1:c.1560C>G	NP_001164105.1:p.Arg520=
NM_001170937.1:c.1551C>G	NP_001164408.1:p.Arg517=
NM_004960.3:c.1563C>G , LRG_655t1:c.1563C>G	NP_004951.1:p.Arg521=
NR_028388.2:n.1633C>G
XM_005255233.3:c.948C>G	XP_005255290.1:p.Arg316=
XM_011545781.1:c.1557C>G	XP_011544083.1:p.Arg519=
XM_011545782.1:c.948C>G	XP_011544084.1:p.Arg316=
XM_005255233.5:c.948C>G	XP_005255290.1:p.Arg316=
XM_011545782.2:c.948C>G	XP_011544084.1:p.Arg316=
XM_024450221.1:c.1554C>G	XP_024305989.1:p.Arg518=
NM_004960.4:c.1563C>G MANE Select	NP_004951.1:p.Arg521=