Canonical Allele Identifier: CA395677378

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31202732A>C (hg19) ; chr16:g.31191411A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31191411A>C , CM000678.2:g.31191411A>C	GRCh38
NC_000016.9:g.31202732A>C , CM000678.1:g.31202732A>C	GRCh37
NC_000016.8:g.31110233A>C	NCBI36
NG_012889.2:g.16280A>C , LRG_655:g.16280A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000254108.12:c.1554A>C MANE Select	ENSP00000254108.8:p.Arg518Ser
ENST00000254108.11:c.1554A>C	ENSP00000254108.7:p.Arg518Ser
ENST00000380244.7:c.1551A>C	ENSP00000369594.3:p.Arg517Ser
ENST00000483853.1:n.631A>C
ENST00000487509.6:n.4729A>C
ENST00000566605.5:c.*727A>C	ENSP00000455073.1:n.*727A>C
ENST00000568685.1:c.1557A>C	ENSP00000455282.1:p.Arg519Ser
ENST00000569760.5:n.445A>C
NM_001170634.1:c.1551A>C	NP_001164105.1:p.Arg517Ser
NM_001170937.1:c.1542A>C	NP_001164408.1:p.Arg514Ser
NM_004960.3:c.1554A>C , LRG_655t1:c.1554A>C	NP_004951.1:p.Arg518Ser
NR_028388.2:n.1624A>C
XM_005255233.3:c.939A>C	XP_005255290.1:p.Arg313Ser
XM_011545781.1:c.1548A>C	XP_011544083.1:p.Arg516Ser
XM_011545782.1:c.939A>C	XP_011544084.1:p.Arg313Ser
XM_005255233.5:c.939A>C	XP_005255290.1:p.Arg313Ser
XM_011545782.2:c.939A>C	XP_011544084.1:p.Arg313Ser
XM_024450221.1:c.1545A>C	XP_024305989.1:p.Arg515Ser
NM_004960.4:c.1554A>C MANE Select	NP_004951.1:p.Arg518Ser