Canonical Allele Identifier: CA2532326174

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189266_31189267insTAAAAA , CM000678.2:g.31189266_31189267insTAAAAA	GRCh38
NC_000016.9:g.31200587_31200588insTAAAAA , CM000678.1:g.31200587_31200588insTAAAAA	GRCh37
NC_000016.8:g.31108088_31108089insTAAAAA	NCBI36
NG_012889.2:g.14135_14136insTAAAAA , LRG_655:g.14135_14136insTAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.936+40_936+41insTAAAAA MANE Select	ENSP00000254108.8:n.936+40_936+41insTAAAAA
ENST00000254108.11:c.936+40_936+41insTAAAAA	ENSP00000254108.7:n.936+40_936+41insTAAAAA
ENST00000380244.7:c.933+40_933+41insTAAAAA	ENSP00000369594.3:n.933+40_933+41insTAAAAA
ENST00000474990.5:n.230+40_230+41insTAAAAA
ENST00000487509.6:n.4111+40_4111+41insTAAAAA
ENST00000564766.1:n.760+40_760+41insTAAAAA
ENST00000566605.5:c.*109+40_*109+41insTAAAAA	ENSP00000455073.1:n.*109+40_*109+41insTAAAAA
ENST00000568685.1:c.939+40_939+41insTAAAAA	ENSP00000455282.1:n.939+40_939+41insTAAAAA
ENST00000568901.2:n.310+40_310+41insTAAAAA
NM_001170634.1:c.933+40_933+41insTAAAAA	NP_001164105.1:n.933+40_933+41insTAAAAA
NM_001170937.1:c.924+40_924+41insTAAAAA	NP_001164408.1:n.924+40_924+41insTAAAAA
NM_004960.3:c.936+40_936+41insTAAAAA , LRG_655t1:c.936+40_936+41insTAAAAA	NP_004951.1:n.936+40_936+41insTAAAAA
NR_028388.2:n.1006+40_1006+41insTAAAAA
XM_005255233.3:c.321+40_321+41insTAAAAA	XP_005255290.1:n.321+40_321+41insTAAAAA
XM_011545781.1:c.930+40_930+41insTAAAAA	XP_011544083.1:n.930+40_930+41insTAAAAA
XM_011545782.1:c.321+40_321+41insTAAAAA	XP_011544084.1:n.321+40_321+41insTAAAAA
XM_005255233.5:c.321+40_321+41insTAAAAA	XP_005255290.1:n.321+40_321+41insTAAAAA
XM_011545782.2:c.321+40_321+41insTAAAAA	XP_011544084.1:n.321+40_321+41insTAAAAA
XM_024450221.1:c.927+40_927+41insTAAAAA	XP_024305989.1:n.927+40_927+41insTAAAAA
NM_004960.4:c.936+40_936+41insTAAAAA MANE Select	NP_004951.1:n.936+40_936+41insTAAAAA