Canonical Allele Identifier: CA395669742

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31196327A>C (hg19) ; chr16:g.31185006A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31185006A>C , CM000678.2:g.31185006A>C	GRCh38
NC_000016.9:g.31196327A>C , CM000678.1:g.31196327A>C	GRCh37
NC_000016.8:g.31103828A>C	NCBI36
NG_012889.2:g.9875A>C , LRG_655:g.9875A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.591A>C MANE Select	ENSP00000254108.8:p.Gln197His
ENST00000254108.11:c.591A>C	ENSP00000254108.7:p.Gln197His
ENST00000380244.7:c.588A>C	ENSP00000369594.3:p.Gln196His
ENST00000487509.6:n.656A>C
ENST00000566605.5:c.591A>C	ENSP00000455073.1:p.Gln197His
ENST00000568685.1:c.591A>C	ENSP00000455282.1:p.Gln197His
NM_001170634.1:c.588A>C	NP_001164105.1:p.Gln196His
NM_001170937.1:c.579A>C	NP_001164408.1:p.Gln193His
NM_004960.3:c.591A>C , LRG_655t1:c.591A>C	NP_004951.1:p.Gln197His
NR_028388.2:n.696A>C
XM_005255233.3:c.11A>C	XP_005255290.1:p.Lys4Thr
XM_011545781.1:c.585A>C	XP_011544083.1:p.Gln195His
XM_011545782.1:c.11A>C	XP_011544084.1:p.Lys4Thr
XM_005255233.5:c.11A>C	XP_005255290.1:p.Lys4Thr
XM_011545782.2:c.11A>C	XP_011544084.1:p.Lys4Thr
XM_024450221.1:c.582A>C	XP_024305989.1:p.Gln194His
NM_004960.4:c.591A>C MANE Select	NP_004951.1:p.Gln197His