Canonical Allele Identifier: CA8023873

Gene: FUS

Linked Data

• dbSNP Id: rs754343013
• ExAC: 16:31200570 GCTTT / G
• gnomAD v2: 16-31200570-GCTTT-G
• gnomAD v3: 16-31189249-GCTTT-G
• gnomAD v4: 16-31189249-GCTTT-G
• MyVariant Identifiers: chr16:g.31200571_31200574del (hg19) ; chr16:g.31189250_31189253del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189252_31189255del , CM000678.2:g.31189252_31189255del	GRCh38
NC_000016.9:g.31200573_31200576del , CM000678.1:g.31200573_31200576del	GRCh37
NC_000016.8:g.31108074_31108077del	NCBI36
NG_012889.2:g.14121_14124del , LRG_655:g.14121_14124del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.936+26_936+29del MANE Select	ENSP00000254108.8:n.936+26_936+29del
ENST00000254108.11:c.936+26_936+29del	ENSP00000254108.7:n.936+26_936+29del
ENST00000380244.7:c.933+26_933+29del	ENSP00000369594.3:n.933+26_933+29del
ENST00000474990.5:n.230+26_230+29del
ENST00000487509.6:n.4111+26_4111+29del
ENST00000564766.1:n.760+26_760+29del
ENST00000566605.5:c.*109+26_*109+29del	ENSP00000455073.1:n.*109+26_*109+29del
ENST00000568685.1:c.939+26_939+29del	ENSP00000455282.1:n.939+26_939+29del
ENST00000568901.2:n.310+26_310+29del
NM_001170634.1:c.933+26_933+29del	NP_001164105.1:n.933+26_933+29del
NM_001170937.1:c.924+26_924+29del	NP_001164408.1:n.924+26_924+29del
NM_004960.3:c.936+26_936+29del , LRG_655t1:c.936+26_936+29del	NP_004951.1:n.936+26_936+29del
NR_028388.2:n.1006+26_1006+29del
XM_005255233.3:c.321+26_321+29del	XP_005255290.1:n.321+26_321+29del
XM_011545781.1:c.930+26_930+29del	XP_011544083.1:n.930+26_930+29del
XM_011545782.1:c.321+26_321+29del	XP_011544084.1:n.321+26_321+29del
XM_005255233.5:c.321+26_321+29del	XP_005255290.1:n.321+26_321+29del
XM_011545782.2:c.321+26_321+29del	XP_011544084.1:n.321+26_321+29del
XM_024450221.1:c.927+26_927+29del	XP_024305989.1:n.927+26_927+29del
NM_004960.4:c.936+26_936+29del MANE Select	NP_004951.1:n.936+26_936+29del