Canonical Allele Identifier: CA2537383834

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189260_31189265del , CM000678.2:g.31189260_31189265del	GRCh38
NC_000016.9:g.31200581_31200586del , CM000678.1:g.31200581_31200586del	GRCh37
NC_000016.8:g.31108082_31108087del	NCBI36
NG_012889.2:g.14129_14134del , LRG_655:g.14129_14134del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.936+34_936+39del MANE Select	ENSP00000254108.8:n.936+34_936+39del
ENST00000254108.11:c.936+34_936+39del	ENSP00000254108.7:n.936+34_936+39del
ENST00000380244.7:c.933+34_933+39del	ENSP00000369594.3:n.933+34_933+39del
ENST00000474990.5:n.230+34_230+39del
ENST00000487509.6:n.4111+34_4111+39del
ENST00000564766.1:n.760+34_760+39del
ENST00000566605.5:c.*109+34_*109+39del	ENSP00000455073.1:n.*109+34_*109+39del
ENST00000568685.1:c.939+34_939+39del	ENSP00000455282.1:n.939+34_939+39del
ENST00000568901.2:n.310+34_310+39del
NM_001170634.1:c.933+34_933+39del	NP_001164105.1:n.933+34_933+39del
NM_001170937.1:c.924+34_924+39del	NP_001164408.1:n.924+34_924+39del
NM_004960.3:c.936+34_936+39del , LRG_655t1:c.936+34_936+39del	NP_004951.1:n.936+34_936+39del
NR_028388.2:n.1006+34_1006+39del
XM_005255233.3:c.321+34_321+39del	XP_005255290.1:n.321+34_321+39del
XM_011545781.1:c.930+34_930+39del	XP_011544083.1:n.930+34_930+39del
XM_011545782.1:c.321+34_321+39del	XP_011544084.1:n.321+34_321+39del
XM_005255233.5:c.321+34_321+39del	XP_005255290.1:n.321+34_321+39del
XM_011545782.2:c.321+34_321+39del	XP_011544084.1:n.321+34_321+39del
XM_024450221.1:c.927+34_927+39del	XP_024305989.1:n.927+34_927+39del
NM_004960.4:c.936+34_936+39del MANE Select	NP_004951.1:n.936+34_936+39del