Canonical Allele Identifier: CA395666343

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31195180A>C (hg19) ; chr16:g.31183859A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31183859A>C , CM000678.2:g.31183859A>C	GRCh38
NC_000016.9:g.31195180A>C , CM000678.1:g.31195180A>C	GRCh37
NC_000016.8:g.31102681A>C	NCBI36
NG_012889.2:g.8728A>C , LRG_655:g.8728A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.192A>C MANE Select	ENSP00000254108.8:p.Thr64=
ENST00000254108.11:c.192A>C	ENSP00000254108.7:p.Thr64=
ENST00000380244.7:c.191-2A>C	ENSP00000369594.3:n.191-2A>C
ENST00000487509.6:n.257A>C
ENST00000487974.1:n.310A>C
ENST00000566605.5:c.192A>C	ENSP00000455073.1:p.Thr64=
ENST00000568685.1:c.192A>C	ENSP00000455282.1:p.Thr64=
NM_001170634.1:c.191-2A>C	NP_001164105.1:n.191-2A>C
NM_001170937.1:c.192A>C	NP_001164408.1:p.Thr64=
NM_004960.3:c.192A>C , LRG_655t1:c.192A>C	NP_004951.1:p.Thr64=
NR_028388.2:n.297A>C
XM_005255233.3:c.-387-2A>C	XP_005255290.1:n.-387-2A>C
XM_011545781.1:c.192A>C	XP_011544083.1:p.Thr64=
XM_005255233.5:c.-387-2A>C	XP_005255290.1:n.-387-2A>C
XM_024450221.1:c.191-2A>C	XP_024305989.1:n.191-2A>C
NM_004960.4:c.192A>C MANE Select	NP_004951.1:p.Thr64=