Canonical Allele Identifier: CA2555889754

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189242_31189243del , CM000678.2:g.31189242_31189243del	GRCh38
NC_000016.9:g.31200563_31200564del , CM000678.1:g.31200563_31200564del	GRCh37
NC_000016.8:g.31108064_31108065del	NCBI36
NG_012889.2:g.14111_14112del , LRG_655:g.14111_14112del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.936+16_936+17del MANE Select	ENSP00000254108.8:n.936+16_936+17del
ENST00000254108.11:c.936+16_936+17del	ENSP00000254108.7:n.936+16_936+17del
ENST00000380244.7:c.933+16_933+17del	ENSP00000369594.3:n.933+16_933+17del
ENST00000474990.5:n.230+16_230+17del
ENST00000487509.6:n.4111+16_4111+17del
ENST00000564766.1:n.760+16_760+17del
ENST00000566605.5:c.*109+16_*109+17del	ENSP00000455073.1:n.*109+16_*109+17del
ENST00000568685.1:c.939+16_939+17del	ENSP00000455282.1:n.939+16_939+17del
ENST00000568901.2:n.310+16_310+17del
NM_001170634.1:c.933+16_933+17del	NP_001164105.1:n.933+16_933+17del
NM_001170937.1:c.924+16_924+17del	NP_001164408.1:n.924+16_924+17del
NM_004960.3:c.936+16_936+17del , LRG_655t1:c.936+16_936+17del	NP_004951.1:n.936+16_936+17del
NR_028388.2:n.1006+16_1006+17del
XM_005255233.3:c.321+16_321+17del	XP_005255290.1:n.321+16_321+17del
XM_011545781.1:c.930+16_930+17del	XP_011544083.1:n.930+16_930+17del
XM_011545782.1:c.321+16_321+17del	XP_011544084.1:n.321+16_321+17del
XM_005255233.5:c.321+16_321+17del	XP_005255290.1:n.321+16_321+17del
XM_011545782.2:c.321+16_321+17del	XP_011544084.1:n.321+16_321+17del
XM_024450221.1:c.927+16_927+17del	XP_024305989.1:n.927+16_927+17del
NM_004960.4:c.936+16_936+17del MANE Select	NP_004951.1:n.936+16_936+17del