Canonical Allele Identifier: CA2632839913

Gene: FUS

Linked Data

• gnomAD v4: 16-31189239-A-AGGAGT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189242_31189246dup , CM000678.2:g.31189242_31189246dup	GRCh38
NC_000016.9:g.31200563_31200567dup , CM000678.1:g.31200563_31200567dup	GRCh37
NC_000016.8:g.31108064_31108068dup	NCBI36
NG_012889.2:g.14111_14115dup , LRG_655:g.14111_14115dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.936+16_936+20dup MANE Select	ENSP00000254108.8:n.936+16_936+20dup
ENST00000254108.11:c.936+16_936+20dup	ENSP00000254108.7:n.936+16_936+20dup
ENST00000380244.7:c.933+16_933+20dup	ENSP00000369594.3:n.933+16_933+20dup
ENST00000474990.5:n.230+16_230+20dup
ENST00000487509.6:n.4111+16_4111+20dup
ENST00000564766.1:n.760+16_760+20dup
ENST00000566605.5:c.*109+16_*109+20dup	ENSP00000455073.1:n.*109+16_*109+20dup
ENST00000568685.1:c.939+16_939+20dup	ENSP00000455282.1:n.939+16_939+20dup
ENST00000568901.2:n.310+16_310+20dup
NM_001170634.1:c.933+16_933+20dup	NP_001164105.1:n.933+16_933+20dup
NM_001170937.1:c.924+16_924+20dup	NP_001164408.1:n.924+16_924+20dup
NM_004960.3:c.936+16_936+20dup , LRG_655t1:c.936+16_936+20dup	NP_004951.1:n.936+16_936+20dup
NR_028388.2:n.1006+16_1006+20dup
XM_005255233.3:c.321+16_321+20dup	XP_005255290.1:n.321+16_321+20dup
XM_011545781.1:c.930+16_930+20dup	XP_011544083.1:n.930+16_930+20dup
XM_011545782.1:c.321+16_321+20dup	XP_011544084.1:n.321+16_321+20dup
XM_005255233.5:c.321+16_321+20dup	XP_005255290.1:n.321+16_321+20dup
XM_011545782.2:c.321+16_321+20dup	XP_011544084.1:n.321+16_321+20dup
XM_024450221.1:c.927+16_927+20dup	XP_024305989.1:n.927+16_927+20dup
NM_004960.4:c.936+16_936+20dup MANE Select	NP_004951.1:n.936+16_936+20dup