Canonical Allele Identifier: CA395677454

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31202740G>C (hg19) ; chr16:g.31191419G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31191419G>C , CM000678.2:g.31191419G>C	GRCh38
NC_000016.9:g.31202740G>C , CM000678.1:g.31202740G>C	GRCh37
NC_000016.8:g.31110241G>C	NCBI36
NG_012889.2:g.16288G>C , LRG_655:g.16288G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000254108.12:c.1562G>C MANE Select	ENSP00000254108.8:p.Arg521Pro
ENST00000254108.11:c.1562G>C	ENSP00000254108.7:p.Arg521Pro
ENST00000380244.7:c.1559G>C	ENSP00000369594.3:p.Arg520Pro
ENST00000483853.1:n.639G>C
ENST00000487509.6:n.4737G>C
ENST00000566605.5:c.*735G>C	ENSP00000455073.1:n.*735G>C
ENST00000568685.1:c.1565G>C	ENSP00000455282.1:p.Arg522Pro
ENST00000569760.5:n.453G>C
NM_001170634.1:c.1559G>C	NP_001164105.1:p.Arg520Pro
NM_001170937.1:c.1550G>C	NP_001164408.1:p.Arg517Pro
NM_004960.3:c.1562G>C , LRG_655t1:c.1562G>C	NP_004951.1:p.Arg521Pro
NR_028388.2:n.1632G>C
XM_005255233.3:c.947G>C	XP_005255290.1:p.Arg316Pro
XM_011545781.1:c.1556G>C	XP_011544083.1:p.Arg519Pro
XM_011545782.1:c.947G>C	XP_011544084.1:p.Arg316Pro
XM_005255233.5:c.947G>C	XP_005255290.1:p.Arg316Pro
XM_011545782.2:c.947G>C	XP_011544084.1:p.Arg316Pro
XM_024450221.1:c.1553G>C	XP_024305989.1:p.Arg518Pro
NM_004960.4:c.1562G>C MANE Select	NP_004951.1:p.Arg521Pro