Canonical Allele Identifier: CA2497030167

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31183954_31183958delinsAT , CM000678.2:g.31183954_31183958delinsAT	GRCh38
NC_000016.9:g.31195275_31195279delinsAT , CM000678.1:g.31195275_31195279delinsAT	GRCh37
NC_000016.8:g.31102776_31102780delinsAT	NCBI36
NG_012889.2:g.8823_8827delinsAT , LRG_655:g.8823_8827delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000254108.12:c.287_291delinsAT MANE Select	ENSP00000254108.8:p.Ser96del
ENST00000254108.11:c.287_291delinsAT	ENSP00000254108.7:p.Ser96del
ENST00000380244.7:c.284_288delinsAT	ENSP00000369594.3:p.Ser95del
ENST00000487509.6:n.352_356delinsAT
ENST00000487974.1:n.405_409delinsAT
ENST00000566605.5:c.287_291delinsAT	ENSP00000455073.1:p.Ser96del
ENST00000568685.1:c.287_291delinsAT	ENSP00000455282.1:p.Ser96del
NM_001170634.1:c.284_288delinsAT	NP_001164105.1:p.Ser95del
NM_001170937.1:c.287_291delinsAT	NP_001164408.1:p.Ser96del
NM_004960.3:c.287_291delinsAT , LRG_655t1:c.287_291delinsAT	NP_004951.1:p.Ser96del
NR_028388.2:n.392_396delinsAT
XM_005255233.3:c.-294_-290delinsAT	XP_005255290.1:n.-294_-290delinsAT
XM_011545781.1:c.287_291delinsAT	XP_011544083.1:p.Ser96del
XM_005255233.5:c.-294_-290delinsAT	XP_005255290.1:n.-294_-290delinsAT
XM_024450221.1:c.284_288delinsAT	XP_024305989.1:p.Ser95del
NM_004960.4:c.287_291delinsAT MANE Select	NP_004951.1:p.Ser96del