Canonical Allele Identifier: CA719933784

Gene: FUS

Linked Data

• dbSNP Id: rs1475253819
• gnomAD v3: 16-31189297-CAAGTCTTTA-C
• gnomAD v4: 16-31189297-CAAGTCTTTA-C
• MyVariant Identifiers: chr16:g.31200619_31200627del (hg19) ; chr16:g.31189298_31189306del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189299_31189307del , CM000678.2:g.31189299_31189307del	GRCh38
NC_000016.9:g.31200620_31200628del , CM000678.1:g.31200620_31200628del	GRCh37
NC_000016.8:g.31108121_31108129del	NCBI36
NG_012889.2:g.14168_14176del , LRG_655:g.14168_14176del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.936+73_936+81del MANE Select	ENSP00000254108.8:n.936+73_936+81del
ENST00000254108.11:c.936+73_936+81del	ENSP00000254108.7:n.936+73_936+81del
ENST00000380244.7:c.933+73_933+81del	ENSP00000369594.3:n.933+73_933+81del
ENST00000474990.5:n.230+73_230+81del
ENST00000487509.6:n.4111+73_4111+81del
ENST00000564766.1:n.760+73_760+81del
ENST00000566605.5:c.*109+73_*109+81del	ENSP00000455073.1:n.*109+73_*109+81del
ENST00000568685.1:c.939+73_939+81del	ENSP00000455282.1:n.939+73_939+81del
ENST00000568901.2:n.310+73_310+81del
NM_001170634.1:c.933+73_933+81del	NP_001164105.1:n.933+73_933+81del
NM_001170937.1:c.924+73_924+81del	NP_001164408.1:n.924+73_924+81del
NM_004960.3:c.936+73_936+81del , LRG_655t1:c.936+73_936+81del	NP_004951.1:n.936+73_936+81del
NR_028388.2:n.1006+73_1006+81del
XM_005255233.3:c.321+73_321+81del	XP_005255290.1:n.321+73_321+81del
XM_011545781.1:c.930+73_930+81del	XP_011544083.1:n.930+73_930+81del
XM_011545782.1:c.321+73_321+81del	XP_011544084.1:n.321+73_321+81del
XM_005255233.5:c.321+73_321+81del	XP_005255290.1:n.321+73_321+81del
XM_011545782.2:c.321+73_321+81del	XP_011544084.1:n.321+73_321+81del
XM_024450221.1:c.927+73_927+81del	XP_024305989.1:n.927+73_927+81del
NM_004960.4:c.936+73_936+81del MANE Select	NP_004951.1:n.936+73_936+81del