Canonical Allele Identifier: CA2216948164

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31191089G= , CM000678.2:g.31191089G=	GRCh38
NC_000016.9:g.31202410G= , CM000678.1:g.31202410G=	GRCh37
NC_000016.8:g.31109911G=	NCBI36
NG_012889.2:g.15958G= , LRG_655:g.15958G=

Transcript Alleles

HGVS	Amino-acid Change
NM_004960.4:c.1520G= MANE Select	NP_004951.1:p.Gly507=
ENST00000254108.12:c.1520G= MANE Select	ENSP00000254108.8:p.Gly507=
NM_001170634.1:c.1517G=	NP_001164105.1:p.Gly506=
NM_001170937.1:c.1508G=	NP_001164408.1:p.Gly503=
NM_004960.3:c.1520G= , LRG_655t1:c.1520G=	NP_004951.1:p.Gly507=
NR_028388.2:n.1590G=
ENST00000254108.11:c.1520G=	ENSP00000254108.7:p.Gly507=
ENST00000380244.7:c.1517G=	ENSP00000369594.3:p.Gly506=
ENST00000474990.5:n.814G=
ENST00000483853.1:n.597G=
ENST00000487509.6:n.4695G=
ENST00000566605.5:c.*693G=	ENSP00000455073.1:n.*693G=
ENST00000568685.1:c.1523G=	ENSP00000455282.1:p.Gly508=
ENST00000569760.5:n.411G=
XM_005255233.3:c.905G=	XP_005255290.1:p.Gly302=
XM_005255233.5:c.905G=	XP_005255290.1:p.Gly302=
XM_011545781.1:c.1514G=	XP_011544083.1:p.Gly505=
XM_011545782.1:c.905G=	XP_011544084.1:p.Gly302=
XM_011545782.2:c.905G=	XP_011544084.1:p.Gly302=
XM_024450221.1:c.1511G=	XP_024305989.1:p.Gly504=