Canonical Allele Identifier: CA2216947176

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189195C= , CM000678.2:g.31189195C=	GRCh38
NC_000016.9:g.31200516C= , CM000678.1:g.31200516C=	GRCh37
NC_000016.8:g.31108017C=	NCBI36
NG_012889.2:g.14064C= , LRG_655:g.14064C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.905C= MANE Select	ENSP00000254108.8:p.Ala302=
ENST00000254108.11:c.905C=	ENSP00000254108.7:p.Ala302=
ENST00000380244.7:c.902C=	ENSP00000369594.3:p.Ala301=
ENST00000474990.5:n.199C=
ENST00000487509.6:n.4080C=
ENST00000564766.1:n.729C=
ENST00000566605.5:c.*78C=	ENSP00000455073.1:n.*78C=
ENST00000568685.1:c.908C=	ENSP00000455282.1:p.Ala303=
ENST00000568901.2:n.279C=
NM_001170634.1:c.902C=	NP_001164105.1:p.Ala301=
NM_001170937.1:c.893C=	NP_001164408.1:p.Ala298=
NM_004960.3:c.905C= , LRG_655t1:c.905C=	NP_004951.1:p.Ala302=
NR_028388.2:n.975C=
XM_005255233.3:c.290C=	XP_005255290.1:p.Ala97=
XM_011545781.1:c.899C=	XP_011544083.1:p.Ala300=
XM_011545782.1:c.290C=	XP_011544084.1:p.Ala97=
XM_005255233.5:c.290C=	XP_005255290.1:p.Ala97=
XM_011545782.2:c.290C=	XP_011544084.1:p.Ala97=
XM_024450221.1:c.896C=	XP_024305989.1:p.Ala299=
NM_004960.4:c.905C= MANE Select	NP_004951.1:p.Ala302=