Canonical Allele Identifier: CA2513658805

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189239_31189240insTCTC , CM000678.2:g.31189239_31189240insTCTC	GRCh38
NC_000016.9:g.31200560_31200561insTCTC , CM000678.1:g.31200560_31200561insTCTC	GRCh37
NC_000016.8:g.31108061_31108062insTCTC	NCBI36
NG_012889.2:g.14108_14109insTCTC , LRG_655:g.14108_14109insTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.936+13_936+14insTCTC MANE Select	ENSP00000254108.8:n.936+13_936+14insTCTC
ENST00000254108.11:c.936+13_936+14insTCTC	ENSP00000254108.7:n.936+13_936+14insTCTC
ENST00000380244.7:c.933+13_933+14insTCTC	ENSP00000369594.3:n.933+13_933+14insTCTC
ENST00000474990.5:n.230+13_230+14insTCTC
ENST00000487509.6:n.4111+13_4111+14insTCTC
ENST00000564766.1:n.760+13_760+14insTCTC
ENST00000566605.5:c.*109+13_*109+14insTCTC	ENSP00000455073.1:n.*109+13_*109+14insTCTC
ENST00000568685.1:c.939+13_939+14insTCTC	ENSP00000455282.1:n.939+13_939+14insTCTC
ENST00000568901.2:n.310+13_310+14insTCTC
NM_001170634.1:c.933+13_933+14insTCTC	NP_001164105.1:n.933+13_933+14insTCTC
NM_001170937.1:c.924+13_924+14insTCTC	NP_001164408.1:n.924+13_924+14insTCTC
NM_004960.3:c.936+13_936+14insTCTC , LRG_655t1:c.936+13_936+14insTCTC	NP_004951.1:n.936+13_936+14insTCTC
NR_028388.2:n.1006+13_1006+14insTCTC
XM_005255233.3:c.321+13_321+14insTCTC	XP_005255290.1:n.321+13_321+14insTCTC
XM_011545781.1:c.930+13_930+14insTCTC	XP_011544083.1:n.930+13_930+14insTCTC
XM_011545782.1:c.321+13_321+14insTCTC	XP_011544084.1:n.321+13_321+14insTCTC
XM_005255233.5:c.321+13_321+14insTCTC	XP_005255290.1:n.321+13_321+14insTCTC
XM_011545782.2:c.321+13_321+14insTCTC	XP_011544084.1:n.321+13_321+14insTCTC
XM_024450221.1:c.927+13_927+14insTCTC	XP_024305989.1:n.927+13_927+14insTCTC
NM_004960.4:c.936+13_936+14insTCTC MANE Select	NP_004951.1:n.936+13_936+14insTCTC