Canonical Allele Identifier: CA2806495530

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189234_31189236del , CM000678.2:g.31189234_31189236del	GRCh38
NC_000016.9:g.31200555_31200557del , CM000678.1:g.31200555_31200557del	GRCh37
NC_000016.8:g.31108056_31108058del	NCBI36
NG_012889.2:g.14103_14105del , LRG_655:g.14103_14105del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.936+8_936+10del MANE Select	ENSP00000254108.8:n.936+8_936+10del
ENST00000254108.11:c.936+8_936+10del	ENSP00000254108.7:n.936+8_936+10del
ENST00000380244.7:c.933+8_933+10del	ENSP00000369594.3:n.933+8_933+10del
ENST00000474990.5:n.230+8_230+10del
ENST00000487509.6:n.4111+8_4111+10del
ENST00000564766.1:n.760+8_760+10del
ENST00000566605.5:c.*109+8_*109+10del	ENSP00000455073.1:n.*109+8_*109+10del
ENST00000568685.1:c.939+8_939+10del	ENSP00000455282.1:n.939+8_939+10del
ENST00000568901.2:n.310+8_310+10del
NM_001170634.1:c.933+8_933+10del	NP_001164105.1:n.933+8_933+10del
NM_001170937.1:c.924+8_924+10del	NP_001164408.1:n.924+8_924+10del
NM_004960.3:c.936+8_936+10del , LRG_655t1:c.936+8_936+10del	NP_004951.1:n.936+8_936+10del
NR_028388.2:n.1006+8_1006+10del
XM_005255233.3:c.321+8_321+10del	XP_005255290.1:n.321+8_321+10del
XM_011545781.1:c.930+8_930+10del	XP_011544083.1:n.930+8_930+10del
XM_011545782.1:c.321+8_321+10del	XP_011544084.1:n.321+8_321+10del
XM_005255233.5:c.321+8_321+10del	XP_005255290.1:n.321+8_321+10del
XM_011545782.2:c.321+8_321+10del	XP_011544084.1:n.321+8_321+10del
XM_024450221.1:c.927+8_927+10del	XP_024305989.1:n.927+8_927+10del
NM_004960.4:c.936+8_936+10del MANE Select	NP_004951.1:n.936+8_936+10del