Canonical Allele Identifier: CA2216944222

Gene: FUS

Linked Data

• dbSNP Id: rs2079239459
• gnomAD v4: 16-31184866-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31184870del , CM000678.2:g.31184870del	GRCh38
NC_000016.9:g.31196191del , CM000678.1:g.31196191del	GRCh37
NC_000016.8:g.31103692del	NCBI36
NG_012889.2:g.9739del , LRG_655:g.9739del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.524-69del MANE Select	ENSP00000254108.8:n.524-69del
ENST00000254108.11:c.524-69del	ENSP00000254108.7:n.524-69del
ENST00000380244.7:c.521-69del	ENSP00000369594.3:n.521-69del
ENST00000487509.6:n.589-69del
ENST00000566605.5:c.524-69del	ENSP00000455073.1:n.524-69del
ENST00000568685.1:c.524-69del	ENSP00000455282.1:n.524-69del
NM_001170634.1:c.521-69del	NP_001164105.1:n.521-69del
NM_001170937.1:c.512-69del	NP_001164408.1:n.512-69del
NM_004960.3:c.524-69del , LRG_655t1:c.524-69del	NP_004951.1:n.524-69del
NR_028388.2:n.629-69del
XM_005255233.3:c.-57-69del	XP_005255290.1:n.-57-69del
XM_011545781.1:c.518-69del	XP_011544083.1:n.518-69del
XM_011545782.1:c.-57-69del	XP_011544084.1:n.-57-69del
XM_005255233.5:c.-57-69del	XP_005255290.1:n.-57-69del
XM_011545782.2:c.-57-69del	XP_011544084.1:n.-57-69del
XM_024450221.1:c.515-69del	XP_024305989.1:n.515-69del
NM_004960.4:c.524-69del MANE Select	NP_004951.1:n.524-69del