Canonical Allele Identifier: CA622172590

Gene: FUS

Linked Data

• gnomAD v2: 16-31196241-A-ATTTTTTT
• MyVariant Identifiers: chr16:g.31196244_31196245delinsTTTTTTTCT (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31184922_31184923insTTTTTTT , CM000678.2:g.31184922_31184923insTTTTTTT	GRCh38
NC_000016.9:g.31196243_31196244insTTTTTTT , CM000678.1:g.31196243_31196244insTTTTTTT	GRCh37
NC_000016.8:g.31103744_31103745insTTTTTTT	NCBI36
NG_012889.2:g.9791_9792insTTTTTTT , LRG_655:g.9791_9792insTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.524-17_524-16insTTTTTTT MANE Select	ENSP00000254108.8:n.524-17_524-16insTTTTTTT
ENST00000254108.11:c.524-17_524-16insTTTTTTT	ENSP00000254108.7:n.524-17_524-16insTTTTTTT
ENST00000380244.7:c.521-17_521-16insTTTTTTT	ENSP00000369594.3:n.521-17_521-16insTTTTTTT
ENST00000487509.6:n.589-17_589-16insTTTTTTT
ENST00000566605.5:c.524-17_524-16insTTTTTTT	ENSP00000455073.1:n.524-17_524-16insTTTTTTT
ENST00000568685.1:c.524-17_524-16insTTTTTTT	ENSP00000455282.1:n.524-17_524-16insTTTTTTT
NM_001170634.1:c.521-17_521-16insTTTTTTT	NP_001164105.1:n.521-17_521-16insTTTTTTT
NM_001170937.1:c.512-17_512-16insTTTTTTT	NP_001164408.1:n.512-17_512-16insTTTTTTT
NM_004960.3:c.524-17_524-16insTTTTTTT , LRG_655t1:c.524-17_524-16insTTTTTTT	NP_004951.1:n.524-17_524-16insTTTTTTT
NR_028388.2:n.629-17_629-16insTTTTTTT
XM_005255233.3:c.-57-17_-57-16insTTTTTTT	XP_005255290.1:n.-57-17_-57-16insTTTTTTT
XM_011545781.1:c.518-17_518-16insTTTTTTT	XP_011544083.1:n.518-17_518-16insTTTTTTT
XM_011545782.1:c.-57-17_-57-16insTTTTTTT	XP_011544084.1:n.-57-17_-57-16insTTTTTTT
XM_005255233.5:c.-57-17_-57-16insTTTTTTT	XP_005255290.1:n.-57-17_-57-16insTTTTTTT
XM_011545782.2:c.-57-17_-57-16insTTTTTTT	XP_011544084.1:n.-57-17_-57-16insTTTTTTT
XM_024450221.1:c.515-17_515-16insTTTTTTT	XP_024305989.1:n.515-17_515-16insTTTTTTT
NM_004960.4:c.524-17_524-16insTTTTTTT MANE Select	NP_004951.1:n.524-17_524-16insTTTTTTT