Canonical Allele Identifier: CA2216947229

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189297_31189306delinsCAAGTCTTTA , CM000678.2:g.31189297_31189306delinsCAAGTCTTTA	GRCh38
NC_000016.9:g.31200618_31200627delinsCAAGTCTTTA , CM000678.1:g.31200618_31200627delinsCAAGTCTTTA	GRCh37
NC_000016.8:g.31108119_31108128delinsCAAGTCTTTA	NCBI36
NG_012889.2:g.14166_14175delinsCAAGTCTTTA , LRG_655:g.14166_14175delinsCAAGTCTTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.936+71_936+80delinsCAAGTCTTTA MANE Select	ENSP00000254108.8:n.936+71_936+80delinsCAAGTCTTTA
ENST00000254108.11:c.936+71_936+80delinsCAAGTCTTTA	ENSP00000254108.7:n.936+71_936+80delinsCAAGTCTTTA
ENST00000380244.7:c.933+71_933+80delinsCAAGTCTTTA	ENSP00000369594.3:n.933+71_933+80delinsCAAGTCTTTA
ENST00000474990.5:n.230+71_230+80delinsCAAGTCTTTA
ENST00000487509.6:n.4111+71_4111+80delinsCAAGTCTTTA
ENST00000564766.1:n.760+71_760+80delinsCAAGTCTTTA
ENST00000566605.5:c.*109+71_*109+80delinsCAAGTCTTTA	ENSP00000455073.1:n.*109+71_*109+80delinsCAAGTCTTTA
ENST00000568685.1:c.939+71_939+80delinsCAAGTCTTTA	ENSP00000455282.1:n.939+71_939+80delinsCAAGTCTTTA
ENST00000568901.2:n.310+71_310+80delinsCAAGTCTTTA
NM_001170634.1:c.933+71_933+80delinsCAAGTCTTTA	NP_001164105.1:n.933+71_933+80delinsCAAGTCTTTA
NM_001170937.1:c.924+71_924+80delinsCAAGTCTTTA	NP_001164408.1:n.924+71_924+80delinsCAAGTCTTTA
NM_004960.3:c.936+71_936+80delinsCAAGTCTTTA , LRG_655t1:c.936+71_936+80delinsCAAGTCTTTA	NP_004951.1:n.936+71_936+80delinsCAAGTCTTTA
NR_028388.2:n.1006+71_1006+80delinsCAAGTCTTTA
XM_005255233.3:c.321+71_321+80delinsCAAGTCTTTA	XP_005255290.1:n.321+71_321+80delinsCAAGTCTTTA
XM_011545781.1:c.930+71_930+80delinsCAAGTCTTTA	XP_011544083.1:n.930+71_930+80delinsCAAGTCTTTA
XM_011545782.1:c.321+71_321+80delinsCAAGTCTTTA	XP_011544084.1:n.321+71_321+80delinsCAAGTCTTTA
XM_005255233.5:c.321+71_321+80delinsCAAGTCTTTA	XP_005255290.1:n.321+71_321+80delinsCAAGTCTTTA
XM_011545782.2:c.321+71_321+80delinsCAAGTCTTTA	XP_011544084.1:n.321+71_321+80delinsCAAGTCTTTA
XM_024450221.1:c.927+71_927+80delinsCAAGTCTTTA	XP_024305989.1:n.927+71_927+80delinsCAAGTCTTTA
NM_004960.4:c.936+71_936+80delinsCAAGTCTTTA MANE Select	NP_004951.1:n.936+71_936+80delinsCAAGTCTTTA