Canonical Allele Identifier: CA719933458

Gene: FUS

Linked Data

• dbSNP Id: rs1346976353
• gnomAD v4: 16-31189061-GT-G
• MyVariant Identifiers: chr16:g.31200383del (hg19) ; chr16:g.31189062del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189067del , CM000678.2:g.31189067del	GRCh38
NC_000016.9:g.31200388del , CM000678.1:g.31200388del	GRCh37
NC_000016.8:g.31107889del	NCBI36
NG_012889.2:g.13936del , LRG_655:g.13936del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.833-56del MANE Select	ENSP00000254108.8:n.833-56del
ENST00000254108.11:c.833-56del	ENSP00000254108.7:n.833-56del
ENST00000380244.7:c.830-56del	ENSP00000369594.3:n.830-56del
ENST00000474990.5:n.127-56del
ENST00000487509.6:n.4008-56del
ENST00000564766.1:n.601del
ENST00000566605.5:c.*6-56del	ENSP00000455073.1:n.*6-56del
ENST00000568685.1:c.833-53del	ENSP00000455282.1:n.833-53del
ENST00000568901.2:n.207-56del
NM_001170634.1:c.830-56del	NP_001164105.1:n.830-56del
NM_001170937.1:c.821-56del	NP_001164408.1:n.821-56del
NM_004960.3:c.833-56del , LRG_655t1:c.833-56del	NP_004951.1:n.833-56del
NR_028388.2:n.903-56del
XM_005255233.3:c.218-56del	XP_005255290.1:n.218-56del
XM_011545781.1:c.827-56del	XP_011544083.1:n.827-56del
XM_011545782.1:c.218-56del	XP_011544084.1:n.218-56del
XM_005255233.5:c.218-56del	XP_005255290.1:n.218-56del
XM_011545782.2:c.218-56del	XP_011544084.1:n.218-56del
XM_024450221.1:c.824-56del	XP_024305989.1:n.824-56del
NM_004960.4:c.833-56del MANE Select	NP_004951.1:n.833-56del