Canonical Allele Identifier: CA395672127

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31200480A>C (hg19) ; chr16:g.31189159A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189159A>C , CM000678.2:g.31189159A>C	GRCh38
NC_000016.9:g.31200480A>C , CM000678.1:g.31200480A>C	GRCh37
NC_000016.8:g.31107981A>C	NCBI36
NG_012889.2:g.14028A>C , LRG_655:g.14028A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.869A>C MANE Select	ENSP00000254108.8:p.Gln290Pro
ENST00000254108.11:c.869A>C	ENSP00000254108.7:p.Gln290Pro
ENST00000380244.7:c.866A>C	ENSP00000369594.3:p.Gln289Pro
ENST00000474990.5:n.163A>C
ENST00000487509.6:n.4044A>C
ENST00000564766.1:n.693A>C
ENST00000566605.5:c.*42A>C	ENSP00000455073.1:n.*42A>C
ENST00000568685.1:c.872A>C	ENSP00000455282.1:p.Gln291Pro
ENST00000568901.2:n.243A>C
NM_001170634.1:c.866A>C	NP_001164105.1:p.Gln289Pro
NM_001170937.1:c.857A>C	NP_001164408.1:p.Gln286Pro
NM_004960.3:c.869A>C , LRG_655t1:c.869A>C	NP_004951.1:p.Gln290Pro
NR_028388.2:n.939A>C
XM_005255233.3:c.254A>C	XP_005255290.1:p.Gln85Pro
XM_011545781.1:c.863A>C	XP_011544083.1:p.Gln288Pro
XM_011545782.1:c.254A>C	XP_011544084.1:p.Gln85Pro
XM_005255233.5:c.254A>C	XP_005255290.1:p.Gln85Pro
XM_011545782.2:c.254A>C	XP_011544084.1:p.Gln85Pro
XM_024450221.1:c.860A>C	XP_024305989.1:p.Gln287Pro
NM_004960.4:c.869A>C MANE Select	NP_004951.1:p.Gln290Pro