Canonical Allele Identifier: CA2216947796

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31190398C= , CM000678.2:g.31190398C=	GRCh38
NC_000016.9:g.31201719C= , CM000678.1:g.31201719C=	GRCh37
NC_000016.8:g.31109220C=	NCBI36
NG_012889.2:g.15267C= , LRG_655:g.15267C=

Transcript Alleles

HGVS	Amino-acid Change
NM_004960.4:c.1292C= MANE Select	NP_004951.1:p.Pro431=
ENST00000254108.12:c.1292C= MANE Select	ENSP00000254108.8:p.Pro431=
NM_001170634.1:c.1289C=	NP_001164105.1:p.Pro430=
NM_001170937.1:c.1280C=	NP_001164408.1:p.Pro427=
NM_004960.3:c.1292C= , LRG_655t1:c.1292C=	NP_004951.1:p.Pro431=
NR_028388.2:n.1362C=
ENST00000254108.11:c.1292C=	ENSP00000254108.7:p.Pro431=
ENST00000380244.7:c.1289C=	ENSP00000369594.3:p.Pro430=
ENST00000474990.5:n.586C=
ENST00000483853.1:n.26C=
ENST00000487509.6:n.4467C=
ENST00000566605.5:c.*465C=	ENSP00000455073.1:n.*465C=
ENST00000568685.1:c.1295C=	ENSP00000455282.1:p.Pro432=
ENST00000569760.5:n.183C=
XM_005255233.3:c.677C=	XP_005255290.1:p.Pro226=
XM_005255233.5:c.677C=	XP_005255290.1:p.Pro226=
XM_011545781.1:c.1286C=	XP_011544083.1:p.Pro429=
XM_011545782.1:c.677C=	XP_011544084.1:p.Pro226=
XM_011545782.2:c.677C=	XP_011544084.1:p.Pro226=
XM_024450221.1:c.1283C=	XP_024305989.1:p.Pro428=