Canonical Allele Identifier: CA2632840012

Gene: FUS

Linked Data

• gnomAD v4: 16-31189372-CTTAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189376_31189379del , CM000678.2:g.31189376_31189379del	GRCh38
NC_000016.9:g.31200697_31200700del , CM000678.1:g.31200697_31200700del	GRCh37
NC_000016.8:g.31108198_31108201del	NCBI36
NG_012889.2:g.14245_14248del , LRG_655:g.14245_14248del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.936+150_936+153del MANE Select	ENSP00000254108.8:n.936+150_936+153del
ENST00000254108.11:c.936+150_936+153del	ENSP00000254108.7:n.936+150_936+153del
ENST00000380244.7:c.933+150_933+153del	ENSP00000369594.3:n.933+150_933+153del
ENST00000474990.5:n.230+150_230+153del
ENST00000487509.6:n.4111+150_4111+153del
ENST00000564766.1:n.760+150_760+153del
ENST00000566605.5:c.*109+150_*109+153del	ENSP00000455073.1:n.*109+150_*109+153del
ENST00000568685.1:c.939+150_939+153del	ENSP00000455282.1:n.939+150_939+153del
ENST00000568901.2:n.310+150_310+153del
NM_001170634.1:c.933+150_933+153del	NP_001164105.1:n.933+150_933+153del
NM_001170937.1:c.924+150_924+153del	NP_001164408.1:n.924+150_924+153del
NM_004960.3:c.936+150_936+153del , LRG_655t1:c.936+150_936+153del	NP_004951.1:n.936+150_936+153del
NR_028388.2:n.1006+150_1006+153del
XM_005255233.3:c.321+150_321+153del	XP_005255290.1:n.321+150_321+153del
XM_011545781.1:c.930+150_930+153del	XP_011544083.1:n.930+150_930+153del
XM_011545782.1:c.321+150_321+153del	XP_011544084.1:n.321+150_321+153del
XM_005255233.5:c.321+150_321+153del	XP_005255290.1:n.321+150_321+153del
XM_011545782.2:c.321+150_321+153del	XP_011544084.1:n.321+150_321+153del
XM_024450221.1:c.927+150_927+153del	XP_024305989.1:n.927+150_927+153del
NM_004960.4:c.936+150_936+153del MANE Select	NP_004951.1:n.936+150_936+153del