Canonical Allele Identifier: CA2216948387

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31191431C= , CM000678.2:g.31191431C=	GRCh38
NC_000016.9:g.31202752C= , CM000678.1:g.31202752C=	GRCh37
NC_000016.8:g.31110253C=	NCBI36
NG_012889.2:g.16300C= , LRG_655:g.16300C=

Transcript Alleles

HGVS	Amino-acid Change
NM_004960.4:c.1574C= MANE Select	NP_004951.1:p.Pro525=
ENST00000254108.12:c.1574C= MANE Select	ENSP00000254108.8:p.Pro525=
NM_001170634.1:c.1571C=	NP_001164105.1:p.Pro524=
NM_001170937.1:c.1562C=	NP_001164408.1:p.Pro521=
NM_004960.3:c.1574C= , LRG_655t1:c.1574C=	NP_004951.1:p.Pro525=
NR_028388.2:n.1644C=
ENST00000254108.11:c.1574C=	ENSP00000254108.7:p.Pro525=
ENST00000380244.7:c.1571C=	ENSP00000369594.3:p.Pro524=
ENST00000483853.1:n.651C=
ENST00000487509.6:n.4749C=
ENST00000566605.5:c.*747C=	ENSP00000455073.1:n.*747C=
ENST00000568685.1:c.1577C=	ENSP00000455282.1:p.Pro526=
ENST00000569760.5:n.465C=
XM_005255233.3:c.959C=	XP_005255290.1:p.Pro320=
XM_005255233.5:c.959C=	XP_005255290.1:p.Pro320=
XM_011545781.1:c.1568C=	XP_011544083.1:p.Pro523=
XM_011545782.1:c.959C=	XP_011544084.1:p.Pro320=
XM_011545782.2:c.959C=	XP_011544084.1:p.Pro320=
XM_024450221.1:c.1565C=	XP_024305989.1:p.Pro522=