Canonical Allele Identifier: CA2632840018

Gene: FUS

Linked Data

• gnomAD v4: 16-31189376-GTTACTGT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189379_31189385del , CM000678.2:g.31189379_31189385del	GRCh38
NC_000016.9:g.31200700_31200706del , CM000678.1:g.31200700_31200706del	GRCh37
NC_000016.8:g.31108201_31108207del	NCBI36
NG_012889.2:g.14248_14254del , LRG_655:g.14248_14254del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.936+153_936+159del MANE Select	ENSP00000254108.8:n.936+153_936+159del
ENST00000254108.11:c.936+153_936+159del	ENSP00000254108.7:n.936+153_936+159del
ENST00000380244.7:c.933+153_933+159del	ENSP00000369594.3:n.933+153_933+159del
ENST00000474990.5:n.230+153_230+159del
ENST00000487509.6:n.4111+153_4111+159del
ENST00000564766.1:n.760+153_760+159del
ENST00000566605.5:c.*109+153_*109+159del	ENSP00000455073.1:n.*109+153_*109+159del
ENST00000568685.1:c.939+153_939+159del	ENSP00000455282.1:n.939+153_939+159del
ENST00000568901.2:n.310+153_310+159del
NM_001170634.1:c.933+153_933+159del	NP_001164105.1:n.933+153_933+159del
NM_001170937.1:c.924+153_924+159del	NP_001164408.1:n.924+153_924+159del
NM_004960.3:c.936+153_936+159del , LRG_655t1:c.936+153_936+159del	NP_004951.1:n.936+153_936+159del
NR_028388.2:n.1006+153_1006+159del
XM_005255233.3:c.321+153_321+159del	XP_005255290.1:n.321+153_321+159del
XM_011545781.1:c.930+153_930+159del	XP_011544083.1:n.930+153_930+159del
XM_011545782.1:c.321+153_321+159del	XP_011544084.1:n.321+153_321+159del
XM_005255233.5:c.321+153_321+159del	XP_005255290.1:n.321+153_321+159del
XM_011545782.2:c.321+153_321+159del	XP_011544084.1:n.321+153_321+159del
XM_024450221.1:c.927+153_927+159del	XP_024305989.1:n.927+153_927+159del
NM_004960.4:c.936+153_936+159del MANE Select	NP_004951.1:n.936+153_936+159del