Canonical Allele Identifier: CA2216944805

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31185032G= , CM000678.2:g.31185032G=	GRCh38
NC_000016.9:g.31196353G= , CM000678.1:g.31196353G=	GRCh37
NC_000016.8:g.31103854G=	NCBI36
NG_012889.2:g.9901G= , LRG_655:g.9901G=

Transcript Alleles

HGVS	Amino-acid Change
NM_004960.4:c.617G= MANE Select	NP_004951.1:p.Gly206=
ENST00000254108.12:c.617G= MANE Select	ENSP00000254108.8:p.Gly206=
NM_001170634.1:c.614G=	NP_001164105.1:p.Gly205=
NM_001170937.1:c.605G=	NP_001164408.1:p.Gly202=
NM_004960.3:c.617G= , LRG_655t1:c.617G=	NP_004951.1:p.Gly206=
NR_028388.2:n.722G=
ENST00000254108.11:c.617G=	ENSP00000254108.7:p.Gly206=
ENST00000380244.7:c.614G=	ENSP00000369594.3:p.Gly205=
ENST00000487509.6:n.682G=
ENST00000566605.5:c.617G=	ENSP00000455073.1:p.Gly206=
ENST00000568685.1:c.617G=	ENSP00000455282.1:p.Gly206=
XM_005255233.3:c.37G=	XP_005255290.1:p.Val13=
XM_005255233.5:c.37G=	XP_005255290.1:p.Val13=
XM_011545781.1:c.611G=	XP_011544083.1:p.Gly204=
XM_011545782.1:c.37G=	XP_011544084.1:p.Val13=
XM_011545782.2:c.37G=	XP_011544084.1:p.Val13=
XM_024450221.1:c.608G=	XP_024305989.1:p.Gly203=