Canonical Allele Identifier: CA2216947170

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189166G= , CM000678.2:g.31189166G=	GRCh38
NC_000016.9:g.31200487G= , CM000678.1:g.31200487G=	GRCh37
NC_000016.8:g.31107988G=	NCBI36
NG_012889.2:g.14035G= , LRG_655:g.14035G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.876G= MANE Select	ENSP00000254108.8:p.Leu292=
ENST00000254108.11:c.876G=	ENSP00000254108.7:p.Leu292=
ENST00000380244.7:c.873G=	ENSP00000369594.3:p.Leu291=
ENST00000474990.5:n.170G=
ENST00000487509.6:n.4051G=
ENST00000564766.1:n.700G=
ENST00000566605.5:c.*49G=	ENSP00000455073.1:n.*49G=
ENST00000568685.1:c.879G=	ENSP00000455282.1:p.Leu293=
ENST00000568901.2:n.250G=
NM_001170634.1:c.873G=	NP_001164105.1:p.Leu291=
NM_001170937.1:c.864G=	NP_001164408.1:p.Leu288=
NM_004960.3:c.876G= , LRG_655t1:c.876G=	NP_004951.1:p.Leu292=
NR_028388.2:n.946G=
XM_005255233.3:c.261G=	XP_005255290.1:p.Leu87=
XM_011545781.1:c.870G=	XP_011544083.1:p.Leu290=
XM_011545782.1:c.261G=	XP_011544084.1:p.Leu87=
XM_005255233.5:c.261G=	XP_005255290.1:p.Leu87=
XM_011545782.2:c.261G=	XP_011544084.1:p.Leu87=
XM_024450221.1:c.867G=	XP_024305989.1:p.Leu289=
NM_004960.4:c.876G= MANE Select	NP_004951.1:p.Leu292=