Canonical Allele Identifier: CA8023549

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31183905G>A , CM000678.2:g.31183905G>A	GRCh38
NC_000016.9:g.31195226G>A , CM000678.1:g.31195226G>A	GRCh37
NC_000016.8:g.31102727G>A	NCBI36
NG_012889.2:g.8774G>A , LRG_655:g.8774G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004960.4:c.238G>A MANE Select	NP_004951.1:p.Gly80Ser
ENST00000254108.12:c.238G>A MANE Select	ENSP00000254108.8:p.Gly80Ser
NM_001170634.1:c.235G>A	NP_001164105.1:p.Gly79Ser
NM_001170937.1:c.238G>A	NP_001164408.1:p.Gly80Ser
NM_004960.3:c.238G>A , LRG_655t1:c.238G>A	NP_004951.1:p.Gly80Ser
NR_028388.2:n.343G>A
ENST00000254108.11:c.238G>A	ENSP00000254108.7:p.Gly80Ser
ENST00000380244.7:c.235G>A	ENSP00000369594.3:p.Gly79Ser
ENST00000487509.6:n.303G>A
ENST00000487974.1:n.356G>A
ENST00000566605.5:c.238G>A	ENSP00000455073.1:p.Gly80Ser
ENST00000568685.1:c.238G>A	ENSP00000455282.1:p.Gly80Ser
XM_005255233.3:c.-343G>A	XP_005255290.1:n.-343G>A
XM_005255233.5:c.-343G>A	XP_005255290.1:n.-343G>A
XM_011545781.1:c.238G>A	XP_011544083.1:p.Gly80Ser
XM_024450221.1:c.235G>A	XP_024305989.1:p.Gly79Ser