Canonical Allele Identifier: CA395674718

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31190282G>T , CM000678.2:g.31190282G>T	GRCh38
NC_000016.9:g.31201603G>T , CM000678.1:g.31201603G>T	GRCh37
NC_000016.8:g.31109104G>T	NCBI36
NG_012889.2:g.15151G>T , LRG_655:g.15151G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004960.4:c.1176G>T MANE Select	NP_004951.1:p.Met392Ile
ENST00000254108.12:c.1176G>T MANE Select	ENSP00000254108.8:p.Met392Ile
NM_001170634.1:c.1173G>T	NP_001164105.1:p.Met391Ile
NM_001170937.1:c.1164G>T	NP_001164408.1:p.Met388Ile
NM_004960.3:c.1176G>T , LRG_655t1:c.1176G>T	NP_004951.1:p.Met392Ile
NR_028388.2:n.1246G>T
ENST00000254108.11:c.1176G>T	ENSP00000254108.7:p.Met392Ile
ENST00000380244.7:c.1173G>T	ENSP00000369594.3:p.Met391Ile
ENST00000474990.5:n.470G>T
ENST00000487509.6:n.4351G>T
ENST00000566605.5:c.*349G>T	ENSP00000455073.1:n.*349G>T
ENST00000568685.1:c.1179G>T	ENSP00000455282.1:p.Met393Ile
ENST00000569760.5:n.67G>T
XM_005255233.3:c.561G>T	XP_005255290.1:p.Met187Ile
XM_005255233.5:c.561G>T	XP_005255290.1:p.Met187Ile
XM_011545781.1:c.1170G>T	XP_011544083.1:p.Met390Ile
XM_011545782.1:c.561G>T	XP_011544084.1:p.Met187Ile
XM_011545782.2:c.561G>T	XP_011544084.1:p.Met187Ile
XM_024450221.1:c.1167G>T	XP_024305989.1:p.Met389Ile