Canonical Allele Identifier: CA2632838766

Gene: FUS

Linked Data

• gnomAD v4: 16-31184897-C-CTTTTTTTTTTTTTTTTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31184902_31184903insTTTTTTTTTTTTTTTTTTTTT , CM000678.2:g.31184902_31184903insTTTTTTTTTTTTTTTTTTTTT	GRCh38
NC_000016.9:g.31196223_31196224insTTTTTTTTTTTTTTTTTTTTT , CM000678.1:g.31196223_31196224insTTTTTTTTTTTTTTTTTTTTT	GRCh37
NC_000016.8:g.31103724_31103725insTTTTTTTTTTTTTTTTTTTTT	NCBI36
NG_012889.2:g.9771_9772insTTTTTTTTTTTTTTTTTTTTT , LRG_655:g.9771_9772insTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.524-37_524-36insTTTTTTTTTTTTTTTTTTTTT MANE Select	ENSP00000254108.8:n.524-37_524-36insTTTTTTTTTTTTTTTTTTTTT
ENST00000254108.11:c.524-37_524-36insTTTTTTTTTTTTTTTTTTTTT	ENSP00000254108.7:n.524-37_524-36insTTTTTTTTTTTTTTTTTTTTT
ENST00000380244.7:c.521-37_521-36insTTTTTTTTTTTTTTTTTTTTT	ENSP00000369594.3:n.521-37_521-36insTTTTTTTTTTTTTTTTTTTTT
ENST00000487509.6:n.589-37_589-36insTTTTTTTTTTTTTTTTTTTTT
ENST00000566605.5:c.524-37_524-36insTTTTTTTTTTTTTTTTTTTTT	ENSP00000455073.1:n.524-37_524-36insTTTTTTTTTTTTTTTTTTTTT
ENST00000568685.1:c.524-37_524-36insTTTTTTTTTTTTTTTTTTTTT	ENSP00000455282.1:n.524-37_524-36insTTTTTTTTTTTTTTTTTTTTT
NM_001170634.1:c.521-37_521-36insTTTTTTTTTTTTTTTTTTTTT	NP_001164105.1:n.521-37_521-36insTTTTTTTTTTTTTTTTTTTTT
NM_001170937.1:c.512-37_512-36insTTTTTTTTTTTTTTTTTTTTT	NP_001164408.1:n.512-37_512-36insTTTTTTTTTTTTTTTTTTTTT
NM_004960.3:c.524-37_524-36insTTTTTTTTTTTTTTTTTTTTT , LRG_655t1:c.524-37_524-36insTTTTTTTTTTTTTTTTTTTTT	NP_004951.1:n.524-37_524-36insTTTTTTTTTTTTTTTTTTTTT
NR_028388.2:n.629-37_629-36insTTTTTTTTTTTTTTTTTTTTT
XM_005255233.3:c.-57-37_-57-36insTTTTTTTTTTTTTTTTTTTTT	XP_005255290.1:n.-57-37_-57-36insTTTTTTTTTTTTTTTTTTTTT
XM_011545781.1:c.518-37_518-36insTTTTTTTTTTTTTTTTTTTTT	XP_011544083.1:n.518-37_518-36insTTTTTTTTTTTTTTTTTTTTT
XM_011545782.1:c.-57-37_-57-36insTTTTTTTTTTTTTTTTTTTTT	XP_011544084.1:n.-57-37_-57-36insTTTTTTTTTTTTTTTTTTTTT
XM_005255233.5:c.-57-37_-57-36insTTTTTTTTTTTTTTTTTTTTT	XP_005255290.1:n.-57-37_-57-36insTTTTTTTTTTTTTTTTTTTTT
XM_011545782.2:c.-57-37_-57-36insTTTTTTTTTTTTTTTTTTTTT	XP_011544084.1:n.-57-37_-57-36insTTTTTTTTTTTTTTTTTTTTT
XM_024450221.1:c.515-37_515-36insTTTTTTTTTTTTTTTTTTTTT	XP_024305989.1:n.515-37_515-36insTTTTTTTTTTTTTTTTTTTTT
NM_004960.4:c.524-37_524-36insTTTTTTTTTTTTTTTTTTTTT MANE Select	NP_004951.1:n.524-37_524-36insTTTTTTTTTTTTTTTTTTTTT