Canonical Allele Identifier: CA395675622

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31190962G>T , CM000678.2:g.31190962G>T	GRCh38
NC_000016.9:g.31202283G>T , CM000678.1:g.31202283G>T	GRCh37
NC_000016.8:g.31109784G>T	NCBI36
NG_012889.2:g.15831G>T , LRG_655:g.15831G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004960.4:c.1394-1G>T MANE Select	NP_004951.1:n.1394-1G>T
ENST00000254108.12:c.1394-1G>T MANE Select	ENSP00000254108.8:n.1394-1G>T
NM_001170634.1:c.1391-1G>T	NP_001164105.1:n.1391-1G>T
NM_001170937.1:c.1382-1G>T	NP_001164408.1:n.1382-1G>T
NM_004960.3:c.1394-1G>T , LRG_655t1:c.1394-1G>T	NP_004951.1:n.1394-1G>T
NR_028388.2:n.1464-1G>T
ENST00000254108.11:c.1394-1G>T	ENSP00000254108.7:n.1394-1G>T
ENST00000380244.7:c.1391-1G>T	ENSP00000369594.3:n.1391-1G>T
ENST00000474990.5:n.688-1G>T
ENST00000483853.1:n.471-1G>T
ENST00000487509.6:n.4569-1G>T
ENST00000566605.5:c.*567-1G>T	ENSP00000455073.1:n.*567-1G>T
ENST00000568685.1:c.1397-1G>T	ENSP00000455282.1:n.1397-1G>T
ENST00000569760.5:n.285-1G>T
XM_005255233.3:c.779-1G>T	XP_005255290.1:n.779-1G>T
XM_005255233.5:c.779-1G>T	XP_005255290.1:n.779-1G>T
XM_011545781.1:c.1388-1G>T	XP_011544083.1:n.1388-1G>T
XM_011545782.1:c.779-1G>T	XP_011544084.1:n.779-1G>T
XM_011545782.2:c.779-1G>T	XP_011544084.1:n.779-1G>T
XM_024450221.1:c.1385-1G>T	XP_024305989.1:n.1385-1G>T