Canonical Allele Identifier: CA8023751

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31185091G>A , CM000678.2:g.31185091G>A	GRCh38
NC_000016.9:g.31196412G>A , CM000678.1:g.31196412G>A	GRCh37
NC_000016.8:g.31103913G>A	NCBI36
NG_012889.2:g.9960G>A , LRG_655:g.9960G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004960.4:c.676G>A MANE Select	NP_004951.1:p.Gly226Ser
ENST00000254108.12:c.676G>A MANE Select	ENSP00000254108.8:p.Gly226Ser
NM_001170634.1:c.673G>A	NP_001164105.1:p.Gly225Ser
NM_001170937.1:c.664G>A	NP_001164408.1:p.Gly222Ser
NM_004960.3:c.676G>A , LRG_655t1:c.676G>A	NP_004951.1:p.Gly226Ser
NR_028388.2:n.781G>A
ENST00000254108.11:c.676G>A	ENSP00000254108.7:p.Gly226Ser
ENST00000380244.7:c.673G>A	ENSP00000369594.3:p.Gly225Ser
ENST00000487509.6:n.741G>A
ENST00000566605.5:c.676G>A	ENSP00000455073.1:p.Gly226Ser
ENST00000568685.1:c.676G>A	ENSP00000455282.1:p.Gly226Ser
ENST00000570090.1:n.12G>A
XM_005255233.3:c.96G>A	XP_005255290.1:p.Ala32=
XM_005255233.5:c.96G>A	XP_005255290.1:p.Ala32=
XM_011545781.1:c.670G>A	XP_011544083.1:p.Gly224Ser
XM_011545782.1:c.96G>A	XP_011544084.1:p.Ala32=
XM_011545782.2:c.96G>A	XP_011544084.1:p.Ala32=
XM_024450221.1:c.667G>A	XP_024305989.1:p.Gly223Ser