Canonical Allele Identifier: CA2580091516

Gene: FUS

Linked Data

• ClinVar Variation Id: 1751796
• ClinVar RCV Id: RCV002360344

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31185028_31185036del , CM000678.2:g.31185028_31185036del	GRCh38
NC_000016.9:g.31196349_31196357del , CM000678.1:g.31196349_31196357del	GRCh37
NC_000016.8:g.31103850_31103858del	NCBI36
NG_012889.2:g.9897_9905del , LRG_655:g.9897_9905del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.613_621del MANE Select	ENSP00000254108.8:p.Ser205_Gly207del
ENST00000254108.11:c.613_621del	ENSP00000254108.7:p.Ser205_Gly207del
ENST00000380244.7:c.610_618del	ENSP00000369594.3:p.Ser204_Gly206del
ENST00000487509.6:n.678_686del
ENST00000566605.5:c.613_621del	ENSP00000455073.1:p.Ser205_Gly207del
ENST00000568685.1:c.613_621del	ENSP00000455282.1:p.Ser205_Gly207del
NM_001170634.1:c.610_618del	NP_001164105.1:p.Ser204_Gly206del
NM_001170937.1:c.601_609del	NP_001164408.1:p.Ser201_Gly203del
NM_004960.3:c.613_621del , LRG_655t1:c.613_621del	NP_004951.1:p.Ser205_Gly207del
NR_028388.2:n.718_726del
XM_005255233.3:c.33_41del	XP_005255290.1:p.Ala12_Ala14del
XM_011545781.1:c.607_615del	XP_011544083.1:p.Ser203_Gly205del
XM_011545782.1:c.33_41del	XP_011544084.1:p.Ala12_Ala14del
XM_005255233.5:c.33_41del	XP_005255290.1:p.Ala12_Ala14del
XM_011545782.2:c.33_41del	XP_011544084.1:p.Ala12_Ala14del
XM_024450221.1:c.604_612del	XP_024305989.1:p.Ser202_Gly204del
NM_004960.4:c.613_621del MANE Select	NP_004951.1:p.Ser205_Gly207del