Canonical Allele Identifier: CA395669857

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31185031G>C , CM000678.2:g.31185031G>C	GRCh38
NC_000016.9:g.31196352G>C , CM000678.1:g.31196352G>C	GRCh37
NC_000016.8:g.31103853G>C	NCBI36
NG_012889.2:g.9900G>C , LRG_655:g.9900G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_004960.4:c.616G>C MANE Select	NP_004951.1:p.Gly206Arg
ENST00000254108.12:c.616G>C MANE Select	ENSP00000254108.8:p.Gly206Arg
NM_001170634.1:c.613G>C	NP_001164105.1:p.Gly205Arg
NM_001170937.1:c.604G>C	NP_001164408.1:p.Gly202Arg
NM_004960.3:c.616G>C , LRG_655t1:c.616G>C	NP_004951.1:p.Gly206Arg
NR_028388.2:n.721G>C
ENST00000254108.11:c.616G>C	ENSP00000254108.7:p.Gly206Arg
ENST00000380244.7:c.613G>C	ENSP00000369594.3:p.Gly205Arg
ENST00000487509.6:n.681G>C
ENST00000566605.5:c.616G>C	ENSP00000455073.1:p.Gly206Arg
ENST00000568685.1:c.616G>C	ENSP00000455282.1:p.Gly206Arg
XM_005255233.3:c.36G>C	XP_005255290.1:p.Ala12=
XM_005255233.5:c.36G>C	XP_005255290.1:p.Ala12=
XM_011545781.1:c.610G>C	XP_011544083.1:p.Gly204Arg
XM_011545782.1:c.36G>C	XP_011544084.1:p.Ala12=
XM_011545782.2:c.36G>C	XP_011544084.1:p.Ala12=
XM_024450221.1:c.607G>C	XP_024305989.1:p.Gly203Arg