Canonical Allele Identifier: CA395676130

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31191111G>A , CM000678.2:g.31191111G>A	GRCh38
NC_000016.9:g.31202432G>A , CM000678.1:g.31202432G>A	GRCh37
NC_000016.8:g.31109933G>A	NCBI36
NG_012889.2:g.15980G>A , LRG_655:g.15980G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004960.4:c.1541+1G>A MANE Select	NP_004951.1:n.1541+1G>A
ENST00000254108.12:c.1541+1G>A MANE Select	ENSP00000254108.8:n.1541+1G>A
NM_001170634.1:c.1538+1G>A	NP_001164105.1:n.1538+1G>A
NM_001170937.1:c.1529+1G>A	NP_001164408.1:n.1529+1G>A
NM_004960.3:c.1541+1G>A , LRG_655t1:c.1541+1G>A	NP_004951.1:n.1541+1G>A
NR_028388.2:n.1611+1G>A
ENST00000254108.11:c.1541+1G>A	ENSP00000254108.7:n.1541+1G>A
ENST00000380244.7:c.1538+1G>A	ENSP00000369594.3:n.1538+1G>A
ENST00000483853.1:n.618+1G>A
ENST00000487509.6:n.4716+1G>A
ENST00000566605.5:c.*714+1G>A	ENSP00000455073.1:n.*714+1G>A
ENST00000568685.1:c.1544+1G>A	ENSP00000455282.1:n.1544+1G>A
ENST00000569760.5:n.432+1G>A
XM_005255233.3:c.926+1G>A	XP_005255290.1:n.926+1G>A
XM_005255233.5:c.926+1G>A	XP_005255290.1:n.926+1G>A
XM_011545781.1:c.1535+1G>A	XP_011544083.1:n.1535+1G>A
XM_011545782.1:c.926+1G>A	XP_011544084.1:n.926+1G>A
XM_011545782.2:c.926+1G>A	XP_011544084.1:n.926+1G>A
XM_024450221.1:c.1532+1G>A	XP_024305989.1:n.1532+1G>A