Canonical Allele Identifier: CA2575976312

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31191373_31191377del , CM000678.2:g.31191373_31191377del	GRCh38
NC_000016.9:g.31202694_31202698del , CM000678.1:g.31202694_31202698del	GRCh37
NC_000016.8:g.31110195_31110199del	NCBI36
NG_012889.2:g.16242_16246del , LRG_655:g.16242_16246del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.1542-26_1542-22del MANE Select	ENSP00000254108.8:n.1542-26_1542-22del
ENST00000254108.11:c.1542-26_1542-22del	ENSP00000254108.7:n.1542-26_1542-22del
ENST00000380244.7:c.1539-26_1539-22del	ENSP00000369594.3:n.1539-26_1539-22del
ENST00000483853.1:n.619-26_619-22del
ENST00000487509.6:n.4717-26_4717-22del
ENST00000566605.5:c.*715-26_*715-22del	ENSP00000455073.1:n.*715-26_*715-22del
ENST00000568685.1:c.1545-26_1545-22del	ENSP00000455282.1:n.1545-26_1545-22del
ENST00000569760.5:n.433-26_433-22del
NM_001170634.1:c.1539-26_1539-22del	NP_001164105.1:n.1539-26_1539-22del
NM_001170937.1:c.1530-26_1530-22del	NP_001164408.1:n.1530-26_1530-22del
NM_004960.3:c.1542-26_1542-22del , LRG_655t1:c.1542-26_1542-22del	NP_004951.1:n.1542-26_1542-22del
NR_028388.2:n.1612-26_1612-22del
XM_005255233.3:c.927-26_927-22del	XP_005255290.1:n.927-26_927-22del
XM_011545781.1:c.1536-26_1536-22del	XP_011544083.1:n.1536-26_1536-22del
XM_011545782.1:c.927-26_927-22del	XP_011544084.1:n.927-26_927-22del
XM_005255233.5:c.927-26_927-22del	XP_005255290.1:n.927-26_927-22del
XM_011545782.2:c.927-26_927-22del	XP_011544084.1:n.927-26_927-22del
XM_024450221.1:c.1533-26_1533-22del	XP_024305989.1:n.1533-26_1533-22del
NM_004960.4:c.1542-26_1542-22del MANE Select	NP_004951.1:n.1542-26_1542-22del