Canonical Allele Identifier: CA494713671

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31200496T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189175T>C , CM000678.2:g.31189175T>C	GRCh38
NC_000016.9:g.31200496T>C , CM000678.1:g.31200496T>C	GRCh37
NC_000016.8:g.31107997T>C	NCBI36
NG_012889.2:g.14044T>C , LRG_655:g.14044T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.885T>C MANE Select	ENSP00000254108.8:p.Asn295=
ENST00000254108.11:c.885T>C	ENSP00000254108.7:p.Asn295=
ENST00000380244.7:c.882T>C	ENSP00000369594.3:p.Asn294=
ENST00000474990.5:n.179T>C
ENST00000487509.6:n.4060T>C
ENST00000564766.1:n.709T>C
ENST00000566605.5:c.*58T>C	ENSP00000455073.1:n.*58T>C
ENST00000568685.1:c.888T>C	ENSP00000455282.1:p.Asn296=
ENST00000568901.2:n.259T>C
NM_001170634.1:c.882T>C	NP_001164105.1:p.Asn294=
NM_001170937.1:c.873T>C	NP_001164408.1:p.Asn291=
NM_004960.3:c.885T>C , LRG_655t1:c.885T>C	NP_004951.1:p.Asn295=
NR_028388.2:n.955T>C
XM_005255233.3:c.270T>C	XP_005255290.1:p.Asn90=
XM_011545781.1:c.879T>C	XP_011544083.1:p.Asn293=
XM_011545782.1:c.270T>C	XP_011544084.1:p.Asn90=
XM_005255233.5:c.270T>C	XP_005255290.1:p.Asn90=
XM_011545782.2:c.270T>C	XP_011544084.1:p.Asn90=
XM_024450221.1:c.876T>C	XP_024305989.1:p.Asn292=
NM_004960.4:c.885T>C MANE Select	NP_004951.1:p.Asn295=